| Attention Deficit-Hyperactivity Disorder |
|
Hyperactivity, Attention deficit hyperactivity disorder |
OMIM:143465 |
| Attention Deficit-Hyperactivity Disorder 8 |
|
Attention deficit hyperactivity disorder |
OMIM:619957 |
| Schizophrenia 15 |
|
Hyperactivity |
OMIM:613950 |
| Renal Hypoplasia |
|
Vesicoureteral reflux, Abnormal renal cortex morphology, Hydronephrosis, Renal insufficiency, Rec... |
ORPHA:93101 |
| Potocki-Lupski syndrome (17p11.2 duplication syndrome) |
|
Hyperactivity |
DECIPHER:19 |
| 22q13 deletion syndrome (Phelan-Mcdermid syndrome) |
|
Hyperactivity |
DECIPHER:20 |
| Focal Segmental Glomerulosclerosis 7 |
|
Nephrotic syndrome, Stage 5 chronic kidney disease, Renal hypoplasia, Proteinuria, Focal segmenta... |
OMIM:616002 |
| Hypoparathyroidism, Familial Isolated, 2 |
|
Hyperphosphatemia, Hypocalcemia, Hypocalcemic seizures |
OMIM:618883 |
| Intellectual Developmental Disorder, Autosomal Recessive 3 |
|
Hyperactivity |
OMIM:608443 |
| Oligomeganephronia |
|
Renal tubular atrophy, Abnormal renal cortex morphology, Abnormal nephron morphology, Stage 5 chr... |
ORPHA:2260 |
| Vesicoureteral Reflux 2 |
|
Renal hypoplasia, Vesicoureteral reflux |
OMIM:610878 |
| Congenital Anomalies Of Kidney And Urinary Tract 3 |
|
Vesicoureteral reflux, Multicystic kidney dysplasia, Ectopic kidney, Renal hypoplasia, Hydronephr... |
OMIM:618270 |
| Holzgreve Syndrome |
|
Renal hypoplasia, Renal agenesis |
OMIM:236110 |
| Congenital Anomalies Of Kidney And Urinary Tract 2 |
|
Congenital megaureter, Renal dysplasia, Hydroureter, Ureteropelvic junction obstruction, Renal hy... |
OMIM:143400 |
| Hypoparathyroidism, Familial Isolated, 1 |
|
Hyperphosphatemia, Hypocalcemia, Cataract, Hypocalcemic seizures |
OMIM:146200 |
| Pseudohypoparathyroidism, Type Ii |
|
Hyperphosphatemia, Hypocalcemia |
OMIM:203330 |
| Vertebral, Cardiac, Renal, And Limb Defects Syndrome 3 |
|
Patent ductus arteriosus, Death in infancy, Bilateral renal agenesis, Unilateral renal agenesis, ... |
OMIM:618845 |
| Ichthyosis, Lamellar, Autosomal Dominant |
|
Hyperkeratosis, Pruritus |
OMIM:146750 |
| Tubulointerstitial Kidney Disease, Autosomal Dominant, 4 |
|
Renal tubular atrophy, Hyperechogenic kidneys, Renal hypoplasia, Proteinuria, Focal segmental glo... |
OMIM:613092 |
| Hyperlysinemia, Type I |
|
Hyperlysinemia, Hyperactivity, Ectopia lentis |
OMIM:238700 |
| Renal Tubular Acidosis, Distal, With Nephrocalcinosis, Short Stature, Impaired Intellectual Development, And Distinctive Facies |
|
Renal cortical hyperechogenicity, Beta 2-microglobulinuria, Medullary nephrocalcinosis, Reduced r... |
OMIM:611555 |
| Intellectual Developmental Disorder, X-Linked 72 |
|
Hyperactivity |
OMIM:300271 |
| Ichthyosis Hystrix, Lambert Type |
|
Orthokeratotic hyperkeratosis, Hyperkeratosis |
OMIM:146600 |
| Adenine Phosphoribosyltransferase Deficiency |
|
Urolithiasis, 2,8-dihydroxyadenine crystalluria, Hematuria, Oliguria, Renal insufficiency, Nephro... |
OMIM:614723 |
| Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 5 |
|
Hemolytic-uremic syndrome, Anuria, Acute kidney injury, Stage 5 chronic kidney disease, Hematuria... |
OMIM:612925 |
| Lessel-Kubisch Syndrome |
|
Renal hypoplasia, Renal insufficiency |
OMIM:618681 |
| Hirschsprung Disease With Polydactyly, Renal Agenesis, And Deafness |
|
Unilateral renal agenesis |
OMIM:235740 |
| Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 3 |
|
Hemolytic-uremic syndrome, Anuria, Acute kidney injury, Hematuria, Proteinuria |
OMIM:612923 |
| Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 2 |
|
Hemolytic-uremic syndrome, Anuria, Acute kidney injury, Hematuria, Proteinuria |
OMIM:612922 |
| Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 6 |
|
Hemolytic-uremic syndrome, Anuria, Acute kidney injury, Hematuria, Proteinuria |
OMIM:612926 |
| Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 4 |
|
Hemolytic-uremic syndrome, Anuria, Acute kidney injury, Hematuria, Proteinuria |
OMIM:612924 |
| Renal Tubular Dysgenesis |
|
Abnormality of the urinary system, Anuria, Renotubular dysgenesis |
OMIM:267430 |
| Autosomal Recessive Primary Microcephaly |
|
Vesicoureteral reflux, Unilateral renal agenesis |
ORPHA:2512 |
| Humero-Radio-Ulnar Synostosis |
|
Abnormality of the ureter, Abnormality of the upper urinary tract |
ORPHA:3266 |
| Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, And Hydranencephaly |
|
Ureteral agenesis, Renal dysplasia, Redundant neck skin, Renal cyst, Hydranencephaly, Stillbirth,... |
OMIM:236500 |
| Familial Isolated Hypoparathyroidism Due To Agenesis Of Parathyroid Gland |
|
Hyperphosphatemia, Hypocalcemia, Hypomagnesemia, Hypocalcemic seizures |
ORPHA:2239 |
| Duplication Of Urethra |
|
Vesicoureteral reflux, Urinary incontinence, Penile hypospadias, Anuria, Recurrent urinary tract ... |
ORPHA:237 |
| Bardet-Biedl Syndrome 19 |
|
Renal hypoplasia, Renal insufficiency, Patent ductus arteriosus, Hydronephrosis |
OMIM:615996 |
| Adenine Phosphoribosyltransferase Deficiency |
|
Uric acid nephrolithiasis, Renal insufficiency, Urinary retention, Recurrent urinary tract infect... |
ORPHA:976 |
| Congenital Anomalies Of Kidney And Urinary Tract Syndrome With Or Without Hearing Loss, Abnormal Ears, Or Developmental Delay |
|
Vesicoureteral reflux, Bifid ureter, Renal dysplasia, Renal agenesis, Decreased numbers of nephro... |
OMIM:617641 |
| Vertebral, Cardiac, Renal, And Limb Defects Syndrome 2 |
|
Renal hypoplasia, Unilateral renal agenesis, Patent ductus arteriosus, Chronic kidney disease |
OMIM:617661 |
| Meier-Gorlin Syndrome 8 |
|
Unilateral renal hypoplasia, Nephroptosis |
OMIM:617564 |
| Intellectual Developmental Disorder, Autosomal Dominant 33 |
|
Hyperactivity |
OMIM:616311 |
| Nephronophthisis 13 |
|
Renal interstitial fibrosis, Stage 5 chronic kidney disease, Glomerular subepithelial immune-comp... |
OMIM:614377 |
| Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, And Hyposegmented Lungs |
|
Hydranencephaly, Unilateral renal agenesis |
OMIM:601355 |
| Hypouricemia, Renal, 1 |
|
Urolithiasis, Renal cortical hyperechogenicity, Uric acid nephrolithiasis, Acute kidney injury, R... |
OMIM:220150 |
| Renal Cysts And Diabetes Syndrome |
|
Stage 5 chronic kidney disease, Glycosuria, Abnormality of the kidney, Decreased numbers of nephr... |
OMIM:137920 |
| Cryptorchidism, Unilateral Or Bilateral |
|
Renal agenesis |
OMIM:219050 |
| Intellectual Disability-Expressive Aphasia-Facial Dysmorphism Syndrome |
|
Hyperactivity |
ORPHA:436151 |
| Pseudohypoparathyroidism, Type Ib |
|
Hyperphosphatemia, Hypocalcemia |
OMIM:603233 |
| Malignant Hyperthermia, Susceptibility To, 2 |
|
Hyperphosphatemia, Hyperkalemia, Elevated circulating creatine kinase concentration |
OMIM:154275 |
| Intellectual Developmental Disorder, Autosomal Recessive 71 |
|
Micropenis, Attention deficit hyperactivity disorder, Unilateral renal agenesis |
OMIM:618504 |
| Syndromic Recessive X-Linked Ichthyosis |
|
Renal insufficiency, Attention deficit hyperactivity disorder, Unilateral renal agenesis |
ORPHA:281090 |
| Corneal Dystrophy, Groenouw Type I |
|
Granular corneal dystrophy, Punctate corneal dystrophy, Cataract, Nodular corneal dystrophy |
OMIM:121900 |
| Malignant Hyperthermia, Susceptibility To, 3 |
|
Hyperphosphatemia, Hyperkalemia, Elevated circulating creatine kinase concentration |
OMIM:154276 |
| Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1 |
|
Acute kidney injury, Hemolytic-uremic syndrome, Anuria, Purpura |
OMIM:235400 |
| Ring Chromosome 8 Syndrome |
|
Abnormality of the ureter, Hydronephrosis |
ORPHA:1450 |
| Hypocalcemia, Autosomal Dominant 1 |
|
Hyperphosphatemia, Hypokalemia, Increased circulating renin level, Hypocalcemia, Hypomagnesemia |
OMIM:601198 |
| Autoimmune Hypoparathyroidism |
|
Conjunctivitis, Hypocalcemic tetany, Hyperphosphatemia, Cataract, Hypocalcemic seizures, Hypocalc... |
ORPHA:36913 |
| Cutis Laxa, Autosomal Dominant 3 |
|
Premature skin wrinkling, Unilateral renal agenesis, Cutis laxa |
OMIM:616603 |
| Senior-Loken Syndrome 4 |
|
Stage 5 chronic kidney disease, Polyuria, Nephronophthisis, Polydipsia |
OMIM:606996 |
| Renal Hypodysplasia/Aplasia 3 |
|
Vesicoureteral reflux, Multicystic kidney dysplasia, Renal dysplasia, Renal agenesis, Horseshoe k... |
OMIM:617805 |
| Radial-Renal Syndrome |
|
Ectopic kidney, Unilateral renal agenesis |
OMIM:179280 |
| Mullerian Duct Aplasia, Unilateral Renal Agenesis, And Cervicothoracic Somite Anomalies |
|
Ectopic kidney, Renal agenesis, Unilateral renal agenesis |
OMIM:601076 |
| Hemorrhagic Fever-Renal Syndrome |
|
Tubulointerstitial nephritis, Anuria, Acute tubulointerstitial nephritis, Petechiae, Acute kidney... |
ORPHA:340 |
| Malignant Hyperthermia, Susceptibility To, 1 |
|
Hyperphosphatemia, Hyperkalemia, Elevated circulating creatine kinase concentration |
OMIM:145600 |
| Renal Hypoplasia, Bilateral |
|
Vesicoureteral reflux, Beta 2-microglobulinuria, Microscopic hematuria, Glycosuria, Renal cyst, D... |
ORPHA:97362 |
| Pseudohypoparathyroidism Type 2 |
|
Hyperphosphatemia, Hypocalcemic tetany, Calcinosis, Hypocalcemic seizures, Hypocalcemia |
ORPHA:94090 |
| Lower Limb Malformation-Hypospadias Syndrome |
|
Hypospadias, Abnormality of the ureter |
ORPHA:2487 |
| Aniridia, Partial, With Unilateral Renal Agenesis And Psychomotor Retardation |
|
Unilateral renal agenesis |
OMIM:206750 |
| Renal Caliceal Diverticuli-Deafness Syndrome |
|
Abnormality of the kidney, Hydroureter, Abnormality of the upper urinary tract, Abnormality of th... |
ORPHA:2838 |
| Split-Hand/Foot Malformation 3 |
|
Renal hypoplasia |
OMIM:246560 |
| Renal Coloboma Syndrome |
|
Vesicoureteral reflux, Multicystic kidney dysplasia, Renal dysplasia, Renal hypoplasia, Renal ins... |
ORPHA:1475 |
| Smith-Magenis syndrome |
|
Hyperactivity |
DECIPHER:8 |
| Nephronophthisis-Like Nephropathy 2 |
|
Stage 5 chronic kidney disease, Polyuria, Tubular luminal dilatation, Renal insufficiency, Perigl... |
OMIM:619468 |
| Tubulointerstitial Kidney Disease, Autosomal Dominant, 2 |
|
Tubulointerstitial nephritis, Renal tubular atrophy, Stage 5 chronic kidney disease, Renal cortic... |
OMIM:174000 |
| Chopra-Amiel-Gordon Syndrome |
|
Attention deficit hyperactivity disorder, Unilateral renal agenesis |
OMIM:619504 |
| Intellectual Developmental Disorder, X-Linked 77 |
|
Hyperactivity |
OMIM:300454 |
| Bresek Syndrome |
|
Vesicoureteral reflux, Hypoplasia of the bladder, Renal dysplasia, Renal hypoplasia, Neonatal death |
ORPHA:85284 |
| Intellectual Developmental Disorder, Autosomal Recessive 37 |
|
Hyperactivity |
OMIM:615493 |
| Bladder Exstrophy And Epispadias Complex |
|
Hydroureter, Unilateral renal agenesis, Epispadias, Horseshoe kidney, Bladder exstrophy |
OMIM:600057 |
| Ank3-Related Intellectual Disability-Sleep Disturbance Syndrome |
|
Hyperactivity |
ORPHA:356996 |
| Craniosynostosis-Hydrocephalus-Arnold-Chiari Malformation Type I-Radioulnar Synostosis Syndrome |
|
Patent ductus arteriosus, Renal agenesis, Hypospadias, Renal hypoplasia, Micropenis, Umbilical he... |
ORPHA:171839 |
| Microcephaly, Facial Dysmorphism, Renal Agenesis, And Ambiguous Genitalia Syndrome |
|
Patent ductus arteriosus, Micropenis, Crossed fused renal ectopia, Unilateral renal agenesis |
OMIM:618142 |
| Mitochondrial Complex V (Atp Synthase) Deficiency, Nuclear Type 1 |
|
Aminoaciduria, 3-Methylglutaconic aciduria, Lacticaciduria, Renal hypoplasia, Death in childhood |
OMIM:604273 |
| Blue Diaper Syndrome |
|
Hyperphosphatemia, Hypercalcemia |
ORPHA:94086 |
| Williams-Beuren Region Duplication Syndrome |
|
Patent ductus arteriosus, Attention deficit hyperactivity disorder, Unilateral renal agenesis, Hy... |
OMIM:609757 |
| Hypogonadotropic Hypogonadism 3 With Or Without Anosmia |
|
Micropenis, Unilateral renal agenesis |
OMIM:244200 |
| Verheij Syndrome |
|
Renal cyst, Renal hypoplasia, Renal agenesis |
OMIM:615583 |
| Pseudohypoparathyroidism, Type Ic |
|
Hypocalcemic tetany, Hypocalcemia, Hyperphosphatemia, Cataract |
OMIM:612462 |
| Bardet-Biedl Syndrome 3 |
|
Renal hypoplasia |
OMIM:600151 |
| Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 2 |
|
Renal cortical hyperechogenicity, Patent ductus arteriosus, Anuria, Pyelonephritis, Megacystis, F... |
OMIM:619351 |
| Microcephaly 20, Primary, Autosomal Recessive |
|
Ureteral agenesis, Bilateral renal agenesis, Arrhinencephaly, Attention deficit hyperactivity dis... |
OMIM:617914 |
| Distal Trisomy 6P |
|
Renal hypoplasia, Abnormality of the urinary system, Dry skin, Hydronephrosis |
ORPHA:1745 |
| Thymic-Renal-Anal-Lung Dysplasia |
|
Ureteral agenesis, Renal agenesis, Ureteral dysgenesis |
OMIM:274265 |
| Burn-Mckeown Syndrome |
|
Renal hypoplasia, Unilateral renal agenesis |
OMIM:608572 |
| Ehlers-Danlos Syndrome, Classic-Like |
|
Vesicoureteral reflux, Striae distensae, Unilateral renal agenesis |
OMIM:606408 |
| Beaulieu-Boycott-Innes Syndrome |
|
Patent ductus arteriosus, Horseshoe kidney, Unilateral renal agenesis, Recurrent urinary tract in... |
OMIM:613680 |
| Renal Agenesis |
|
Ureteral agenesis, Renal insufficiency, Bilateral renal agenesis, Renal agenesis, Unilateral rena... |
ORPHA:411709 |
| Joubert Syndrome 22 |
|
Renal hypoplasia |
OMIM:615665 |
| Congenital Disorder Of Glycosylation, Type Iil |
|
Patent ductus arteriosus, Proximal tubulopathy, Death in infancy, Unilateral renal agenesis, Hype... |
OMIM:614576 |
| Alagille Syndrome 2 |
|
Renal insufficiency, Renal tubular acidosis, Hematuria, Renal cyst, Renal hypoplasia, Proteinuria |
OMIM:610205 |
| Cervical Ribs, Sprengel Anomaly, Anal Atresia, And Urethral Obstruction |
|
Renal hypoplasia, Hypertrophy of the urinary bladder, Urethral obstruction, Renal dysplasia |
OMIM:601389 |
| Combined Oxidative Phosphorylation Deficiency 11 |
|
Renal tubular acidosis, Renal dysplasia, Death in infancy, Renal cyst, Renal hypoplasia, Renal in... |
OMIM:614922 |
| Nephronophthisis 1 |
|
Renal tubular atrophy, Hyposthenuria, Stage 5 chronic kidney disease, Renal corticomedullary cyst... |
OMIM:256100 |
| X-Linked Intellectual Disability, Stocco Dos Santos Type |
|
Hyperactivity, Cataract |
ORPHA:85288 |
| Microcephaly, Seizures, And Developmental Delay |
|
Hyperactivity, Ataxia |
OMIM:613402 |
| Inverted Duplicated Chromosome 15 Syndrome |
|
Hyperactivity, Unilateral renal agenesis |
ORPHA:3306 |
| Congenital Hypotonia, Epilepsy, Developmental Delay, And Digital Anomalies |
|
Renal hypoplasia, Dysphagia, Unilateral renal agenesis, Hydronephrosis |
OMIM:618494 |
| Even-Plus Syndrome |
|
Renal hypoplasia, Vesicoureteral reflux, Recurrent urinary tract infections |
OMIM:616854 |
| Renal Glucosuria |
|
Enuresis nocturna, Glycosuria, Polyuria, Polyphagia, Polydipsia |
OMIM:233100 |
| Developmental And Epileptic Encephalopathy 43 |
|
Impulsivity, Hyperactivity, Attention deficit hyperactivity disorder, Ataxia |
OMIM:617113 |
| Congenital Primary Megaureter |
|
Vesicoureteral reflux, Hydronephrosis, Congenital megaureter, Recurrent urinary tract infections,... |
ORPHA:617 |
| Nephronophthisis 4 |
|
Renal tubular atrophy, Stage 5 chronic kidney disease, Renal corticomedullary cysts, Polyuria, Ne... |
OMIM:606966 |
| Hadziselimovic Syndrome |
|
Renal hypoplasia |
OMIM:612946 |
| Fibulo-Ulnar Hypoplasia-Renal Anomalies Syndrome |
|
Renal hypoplasia, Hypoplasia of penis |
ORPHA:2256 |
| Cataract-Microcornea Syndrome |
|
Microcornea, Cataract, Iris coloboma, Corneal opacity, Corneal dystrophy |
ORPHA:1377 |
| Hartnup Disorder |
|
Hyperactivity, Attention deficit hyperactivity disorder, Episodic ataxia |
OMIM:234500 |
| Pseudopseudohypoparathyroidism |
|
Hyperphosphatemia, Hypocalcemia |
ORPHA:79445 |
| Hypercalcemia, Infantile, 2 |
|
Renal phosphate wasting, Medullary nephrocalcinosis, Polyuria, Nephrocalcinosis, Hypercalciuria |
OMIM:616963 |
| Intellectual Developmental Disorder, X-Linked, Syndromic, Houge Type |
|
Impulsivity, Hyperactivity, Attention deficit hyperactivity disorder |
OMIM:301008 |
| Nephronophthisis 3 |
|
Renal tubular atrophy, Stage 5 chronic kidney disease, Renal corticomedullary cysts, Polyuria, Ne... |
OMIM:604387 |
| Vacterl Association With Hydrocephalus |
|
Renal hypoplasia, Stillbirth |
OMIM:276950 |
| Pseudohypoparathyroidism, Type Ia |
|
Hypocalcemic tetany, Hyperphosphatemia, Cataract |
OMIM:103580 |
| Infection-Related Hemolytic Uremic Syndrome |
|
Nephrotic range proteinuria, Anuria, Acute kidney injury, Decreased urine output, Pallor, Oliguria |
ORPHA:544482 |
| Bardet-Biedl Syndrome 16 |
|
Renal dysplasia, Stage 5 chronic kidney disease, Renal agenesis, Renal cyst, Renal insufficiency |
OMIM:615993 |
| Braddock Syndrome |
|
Unilateral renal agenesis |
ORPHA:52047 |
| Coach Syndrome 1 |
|
Multiple small medullary renal cysts, Encephalocele, Stage 5 chronic kidney disease, Unilateral r... |
OMIM:216360 |
| Orofaciodigital Syndrome Xvii |
|
Renal hypoplasia, Micropenis |
OMIM:617926 |
| Renal Tubular Acidosis, Distal, 4, With Hemolytic Anemia |
|
Nephrocalcinosis, Isothenuria, Distal renal tubular acidosis, Pallor |
OMIM:611590 |
| Cenani-Lenz Syndactyly Syndrome |
|
Renal hypoplasia, Renal agenesis, Ectopic kidney |
OMIM:212780 |
| Hyperphosphatasia With Impaired Intellectual Development Syndrome 3 |
|
Hyperphosphatemia |
OMIM:614207 |
| Diffuse Cutaneous Systemic Sclerosis |
|
Renal insufficiency, Skin ulcer, Oliguria, Dysphagia |
ORPHA:220393 |
| Branchiootorenal Syndrome 1 |
|
Renal steatosis, Vesicoureteral reflux, Renal dysplasia, Renal malrotation, Polycystic kidney dys... |
OMIM:113650 |
| Genetic Recurrent Myoglobinuria |
|
Hyperphosphatemia, Highly elevated creatine kinase, Hyperkalemia, Difficulty walking, Hypocalcemia |
ORPHA:99845 |
| Short-Rib Thoracic Dysplasia 5 With Or Without Polydactyly |
|
Stage 5 chronic kidney disease, Chronic tubulointerstitial nephritis, Glomerulonephritis, Renal h... |
OMIM:614376 |
| Renal And Mullerian Duct Hypoplasia |
|
Renal hypoplasia, Horseshoe kidney, Anteriorly displaced urethral meatus |
OMIM:266810 |
| Type 1 Diabetes Mellitus |
|
Polyuria, Polyphagia, Polydipsia |
OMIM:222100 |
| Lassa Fever |
|
Dysphagia, Oliguria, Miscarriage |
ORPHA:99824 |
| Dystonia 31 |
|
Abnormal posturing, Dysphagia |
OMIM:619565 |
| Fanconi Anemia, Complementation Group I |
|
Vesicoureteral reflux, Pallor, Horseshoe kidney, Renal hypoplasia, Abnormal renal morphology |
OMIM:609053 |
| Intellectual Developmental Disorder, Autosomal Dominant 36 |
|
Unilateral renal agenesis |
OMIM:616362 |
| Hyperprolinemia, Type I |
|
Hyperactivity, Hyperprolinemia, Ataxia |
OMIM:239500 |
| Senior-Boichis Syndrome |
|
Stage 5 chronic kidney disease, Renal corticomedullary cysts, Abnormal renal insterstitial morpho... |
ORPHA:84081 |
| Meckel Syndrome 12 |
|
Renal hypoplasia, Arrhinencephaly, Ureteral hypoplasia, Bilateral renal agenesis |
OMIM:616258 |
| Hypophosphatemic Rickets, Autosomal Recessive, 1 |
|
Hypophosphatemia, Hypophosphatemic rickets |
OMIM:241520 |
| Klippel-Feil Syndrome 1, Autosomal Dominant |
|
Abnormality of the kidney, Unilateral renal agenesis |
OMIM:118100 |
| Short Stature-Brachydactyly-Obesity-Global Developmental Delay Syndrome |
|
Renal hypoplasia, Vesicoureteral reflux |
ORPHA:464288 |
| Kallmann Syndrome With Spastic Paraplegia |
|
Micropenis, Unilateral renal agenesis |
OMIM:308750 |
| Cach Syndrome |
|
Renal hypoplasia, Dysphagia |
ORPHA:135 |
| Papillorenal Syndrome |
|
Vesicoureteral reflux, Multicystic kidney dysplasia, Stage 5 chronic kidney disease, Renal malrot... |
OMIM:120330 |
| Senior-Loken Syndrome 8 |
|
Stage 5 chronic kidney disease, Pallor, Glomerular subepithelial immune-complex deposits, Global ... |
OMIM:616307 |
| Glycine Encephalopathy |
|
Restlessness, Impulsivity, Hyperactivity, Hyperglycinemia |
OMIM:605899 |
| Hypercalcemia, Infantile, 1 |
|
Medullary nephrocalcinosis, Polyuria, Nephrocalcinosis, Nephrolithiasis, Hypercalciuria |
OMIM:143880 |
| Vertebral, Cardiac, Tracheoesophageal, Renal, And Limb Defects |
|
Spina bifida occulta, Renal agenesis, Attention deficit hyperactivity disorder, Unilateral renal ... |
OMIM:619227 |
| Developmental And Epileptic Encephalopathy 104 |
|
Hyperactivity, Agitation |
OMIM:619970 |
| Hereditary Persistence Of Fetal Hemoglobin-Beta-Thalassemia Syndrome |
|
Pallor |
ORPHA:46532 |
| Pseudohypoparathyroidism Type 1B |
|
Conjunctivitis, Hypocalcemic tetany, Hyperphosphatemia, Calcinosis, Cataract, Hypocalcemic seizur... |
ORPHA:94089 |
| Calciphylaxis |
|
Hyperphosphatemia |
ORPHA:280062 |
| Mayer-Rokitansky-Küster-Hauser Syndrome |
|
Ectopic kidney, Abnormality of the kidney, Horseshoe kidney, Unilateral renal agenesis |
ORPHA:3109 |
| Thoc6-Related Developmental Delay-Microcephaly-Facial Dysmorphism Syndrome |
|
Patent ductus arteriosus, Recurrent urinary tract infections, Abnormality of the kidney, Unilater... |
ORPHA:363444 |
| Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 |
|
Conjunctival whitish salt-like deposits, Hyperphosphatemia, Calcinosis |
OMIM:211900 |
| Shiga Toxin-Associated Hemolytic Uremic Syndrome |
|
Acute kidney injury, Hemoglobinuria, Anuria |
ORPHA:90038 |
| Microscopic Polyangiitis |
|
Glomerulopathy, Skin ulcer, Hematuria, Oliguria, Erythema, Renal insufficiency |
ORPHA:727 |
| Sanjad-Sakati Syndrome |
|
Astigmatism, Hypocalcemia, Corneal opacity, Hyperphosphatemia |
ORPHA:2323 |
| Deafness-Intellectual Disability Syndrome, Martin-Probst Type |
|
Renal dysplasia, Hypoplasia of penis, Renal hypoplasia, Renal insufficiency, Umbilical hernia |
ORPHA:85321 |
| Adams-Oliver Syndrome 6 |
|
Renal hypoplasia |
OMIM:616589 |
| Systemic Capillary Leak Syndrome |
|
Abnormal renal tubule morphology, Renal insufficiency, Oliguria |
ORPHA:188 |
| Mungan Syndrome |
|
Renal hypoplasia, Vesicoureteral reflux |
OMIM:611376 |
| Methylmalonic Acidemia With Homocystinuria, Type Cbld |
|
Pallor |
ORPHA:79283 |
| Mitochondrial Complex Iv Deficiency, Nuclear Type 10 |
|
Renal hypoplasia, Ketonuria |
OMIM:619053 |
| Congenital Megacalycosis |
|
Tubulointerstitial nephritis, Dilatation of renal calices, Recurrent urinary tract infections, En... |
ORPHA:93109 |
| Emanuel Syndrome |
|
Patent ductus arteriosus, Unilateral renal agenesis, Redundant neck skin, Dysphagia, Renal hypopl... |
ORPHA:96170 |
| Dworschak-Punetha Neurodevelopmental Syndrome |
|
Vesicoureteral reflux, Unilateral renal hypoplasia |
OMIM:619955 |
| Brain Malformations With Or Without Urinary Tract Defects |
|
Renal hypoplasia, Vesicoureteral reflux, Hydronephrosis |
OMIM:613735 |
| Lethal Hemolytic Anemia-Genital Anomalies Syndrome |
|
Renal hypoplasia/aplasia, Hypospadias, Abnormality of the ureter, Hypoplasia of penis |
ORPHA:1046 |
| Morm Syndrome |
|
Hyperactivity, Cataract |
ORPHA:75858 |
| Tumoral Calcinosis, Hyperphosphatemic, Familial, 3 |
|
Hyperphosphatemia, Hypercalcemia |
OMIM:617994 |
| Senior-Loken Syndrome 1 |
|
Impaired renal concentrating ability, Stage 5 chronic kidney disease, Thickening of the tubular b... |
OMIM:266900 |
| Peripheral Cone Dystrophy |
|
Pallor |
OMIM:609021 |
| Hypomagnesemia, Seizures, And Impaired Intellectual Development 2 |
|
Hyperactivity, Polyuria, Renal magnesium wasting, Nephrocalcinosis, Renal potassium wasting |
OMIM:618314 |
| Emanuel Syndrome |
|
Patent ductus arteriosus, Recurrent urinary tract infections, Unilateral renal agenesis, Renal hy... |
OMIM:609029 |
| Neurodevelopmental, Jaw, Eye, And Digital Syndrome |
|
Renal hypoplasia, Impulsivity, Umbilical hernia |
OMIM:618914 |
| Kenny-Caffey Syndrome, Type 2 |
|
Developmental cataract, Hypocalcemia, Hyperphosphatemia, Transient hypophosphatemia |
OMIM:127000 |
| Primary Lateral Sclerosis, Juvenile |
|
Dysphagia, Pseudobulbar paralysis, Pallor |
OMIM:606353 |
| Senior-Loken Syndrome 3 |
|
Stage 5 chronic kidney disease, Renal corticomedullary cysts, Polyuria, Nephronophthisis, Enuresi... |
OMIM:606995 |
| Aniridia-Renal Agenesis-Psychomotor Retardation Syndrome |
|
Unilateral renal agenesis |
ORPHA:1064 |
| Megalocornea |
|
Mosaic corneal dystrophy, Megalocornea, Corneal arcus, Iris transillumination defect, Deep anteri... |
OMIM:309300 |
| Pseudohypoparathyroidism Type 1C |
|
Conjunctivitis, Hypocalcemic tetany, Hyperphosphatemia, Calcinosis, Cataract, Polyphagia, Hypocal... |
ORPHA:79444 |
| Cone-Rod Dystrophy 11 |
|
Pallor |
OMIM:610381 |
| Microcephaly, Short Stature, And Impaired Glucose Metabolism 2 |
|
Renal hypoplasia |
OMIM:616817 |
| Linear Verrucous Nevus Syndrome |
|
Abnormal cornea morphology, Hypophosphatemia, Iris coloboma, Cataract |
ORPHA:2611 |
| Intellectual Developmental Disorder, X-Linked 109 |
|
Impulsivity, Hyperactivity, Agitation |
OMIM:309548 |
| Hypoparathyroidism-Retardation-Dysmorphism Syndrome |
|
Hypocalcemia, Hyperphosphatemia, Hypocalcemic seizures |
OMIM:241410 |
| Birk-Landau-Perez Syndrome |
|
Tubulointerstitial nephritis, Stage 3 chronic kidney disease, Renal hypoplasia, Renal insufficien... |
OMIM:617595 |
| Neuroleptic Malignant Syndrome |
|
Hyperphosphatemia, Hyperuricemia, Hyperkalemia, Agitation, Elevated circulating creatine kinase c... |
ORPHA:94093 |
| Mannosidosis, Beta A, Lysosomal |
|
Tortuosity of conjunctival vessels, Hyperactivity |
OMIM:248510 |
| Exfoliation Syndrome |
|
Phakodonesis, Pigment deposition in the trabecular meshwork, Mydriasis, Iris hypoperfusion, Lens ... |
OMIM:177650 |
| Fraser Syndrome 2 |
|
Aplasia of the bladder, Renal agenesis, Renal hypoplasia |
OMIM:617666 |
| Nephronophthisis 11 |
|
Renal tubular atrophy, Stage 5 chronic kidney disease, Renal corticomedullary cysts, Tubular base... |
OMIM:613550 |
| Fanconi Anemia, Complementation Group W |
|
Renal hypoplasia |
OMIM:617784 |
| Distal Limb Deficiencies-Micrognathia Syndrome |
|
Renal hypoplasia, Renal insufficiency, Proteinuria |
ORPHA:1307 |
| Phenylketonuria |
|
Hyperactivity, Hyperphenylalaninemia, Maternal hyperphenylalaninemia, Cataract, Attention deficit... |
OMIM:261600 |
| Vitamin D-Dependent Rickets, Type 3 |
|
Hypophosphatemia, Hypocalcemia |
OMIM:619073 |
| Tessadori-Bicknell-Van Haaften Neurodevelopmental Syndrome 4 |
|
Vesicoureteral reflux, Micropenis, Unilateral renal agenesis |
OMIM:619951 |
| Shashi-Pena Syndrome |
|
Patent ductus arteriosus, Unilateral renal agenesis |
OMIM:617190 |
| Hypogonadotropic Hypogonadism 1 With Or Without Anosmia |
|
Micropenis, Unilateral renal agenesis |
OMIM:308700 |
| Intellectual Developmental Disorder, X-Linked 101 |
|
Hyperactivity |
OMIM:300928 |
| Pseudohypoparathyroidism Type 1A |
|
Conjunctivitis, Hypocalcemic tetany, Hyperphosphatemia, Calcinosis, Choreoathetosis, Cataract, Po... |
ORPHA:79443 |
| Nager Syndrome |
|
Unilateral renal agenesis |
ORPHA:245 |
| Intellectual Developmental Disorder, Autosomal Dominant 67 |
|
Astigmatism, Hyperactivity, Attention deficit hyperactivity disorder |
OMIM:619927 |
| Fraxe Intellectual Disability |
|
Hyperactivity, Impulsivity, Agitation |
ORPHA:100973 |
| 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency |
|
Increased level of 3-hydroxy-3-methylglutaric acid in urine, Organic aciduria, Pallor, Increased ... |
OMIM:246450 |
| Vertebral, Cardiac, Renal, And Limb Defects Syndrome 1 |
|
Renal hypoplasia, Vesicoureteral reflux, Spinal dysraphism |
OMIM:617660 |
| Beta-Mercaptolactate Cysteine Disulfiduria |
|
Abnormality of the ureter, Dry skin, Umbilical hernia |
ORPHA:1035 |
| Chromosome 17Q12 Deletion Syndrome |
|
Pica, Multicystic kidney dysplasia, Hypoplasia of the bladder, Recurrent urinary tract infections... |
OMIM:614527 |
| Retinitis Pigmentosa 51 |
|
Abnormality of the kidney, Pallor |
OMIM:613464 |
| Brain Malformation-Congenital Heart Disease-Postaxial Polydactyly Syndrome |
|
Renal hypoplasia |
ORPHA:75389 |
| Matthew-Wood Syndrome |
|
Renal hypoplasia, Vesicoureteral reflux, Horseshoe kidney |
ORPHA:2470 |
| Anterior Segment Dysgenesis 8 |
|
Iris transillumination defect, Persistent pupillary membrane, Hypoplasia of the iris, Uveal ectro... |
OMIM:617319 |
| Acute Peripheral Arterial Occlusion |
|
Pallor |
ORPHA:90064 |
| Renal Dysplasia |
|
Vesicovaginal fistula, Congenital posterior urethral valve, Moderate proteinuria, Abnormal renal ... |
ORPHA:93108 |
| Optic Atrophy 1 |
|
Pallor |
OMIM:165500 |
| Encephalopathy, Progressive, With Or Without Lipodystrophy |
|
Hyperactivity, Hypertriglyceridemia, Ataxia |
OMIM:615924 |
| Intellectual Developmental Disorder, X-Linked, Syndromic, Pilorge Type |
|
Hyperactivity |
OMIM:301076 |
| Prune Belly Syndrome With Pulmonic Stenosis, Mental Retardation, And Deafness |
|
Hydroureter, Hydronephrosis |
OMIM:264140 |
| Genetic Hyperferritinemia Without Iron Overload |
|
Abnormal serum iron concentration, Cataract, Increased circulating ferritin concentration, Elevat... |
ORPHA:254704 |
| Sepsis In Premature Infants |
|
Petechiae, Purpura, Pallor, Reversible renal failure, Oliguria |
ORPHA:90051 |
| Dysmyelination With Jaundice |
|
Hydroureter, Hypoplasia of penis, Hydronephrosis |
OMIM:224250 |
| 8p23.1 deletion syndrome |
|
Hyperactivity |
DECIPHER:39 |
| Short Stature, Microcephaly, And Endocrine Dysfunction |
|
Renal hypoplasia, Micropenis, Unilateral renal agenesis, Ectopic kidney |
OMIM:616541 |
| Acute Monoblastic/Monocytic Leukemia |
|
Oliguria |
ORPHA:514 |
| Dermatitis, Atopic |
|
Facial erythema, Dry skin, Pallor |
OMIM:603165 |
| Intellectual Developmental Disorder With Epilepsy, Behavioral Abnormalities, And Coarse Facies |
|
Hyperactivity |
OMIM:619031 |
| Bifid Nose With Or Without Anorectal And Renal Anomalies |
|
Renal agenesis, Unilateral renal agenesis |
OMIM:608980 |
| Benign Paroxysmal Torticollis Of Infancy |
|
Pallor |
ORPHA:71518 |
| Mullerian Aplasia And Hyperandrogenism |
|
Unilateral renal agenesis |
OMIM:158330 |
| Autoimmune Hemolytic Anemia, Cold Type |
|
Pallor |
ORPHA:228312 |
| Neurodevelopmental Disorder With Epilepsy And Hypoplasia Of The Corpus Callosum |
|
Gait ataxia, Hyperactivity, Inability to walk, Gait disturbance, Dysmetria |
OMIM:618090 |
| Non-Functioning Paraganglioma |
|
Hematuria, Elevated urinary epinephrine, Pallor, Elevated urinary dopamine, Elevated urinary nore... |
ORPHA:94080 |
| Idiopathic Steroid-Resistant Nephrotic Syndrome |
|
Abnormal urine output, Acute kidney injury, Stage 5 chronic kidney disease, Minimal change glomer... |
ORPHA:567548 |
| Tessadori-Bicknell-Van Haaften Neurodevelopmental Syndrome 1 |
|
Renal hypoplasia, Umbilical hernia, Absence of renal corticomedullary differentiation |
OMIM:619758 |
| Vesicoureteral Reflux 3 |
|
Ureter duplex, Recurrent urinary tract infections, Hydroureter, Grade IV vesicoureteral reflux, G... |
OMIM:613674 |
| 12Q14 Microdeletion Syndrome |
|
Renal hypoplasia, Horseshoe kidney, Ectopic kidney |
ORPHA:94063 |
| Retinitis Pigmentosa 27 |
|
Pallor |
OMIM:613750 |
| Rauch-Steindl Syndrome |
|
Hyperactivity, Hyperechogenic kidneys, Bilateral renal hypoplasia, Miscarriage |
OMIM:619695 |
| Methylmalonic Acidemia With Homocystinuria Type Cblf |
|
Methylmalonic aciduria, Unilateral renal agenesis |
ORPHA:79284 |
| Penoscrotal Transposition |
|
Renal dysplasia, Penoscrotal transposition, Renal agenesis, Abnormality of the ureter, Hypospadia... |
ORPHA:2842 |
| Myopathy, Lactic Acidosis, And Sideroblastic Anemia 2 |
|
Dysphagia, Pallor |
OMIM:613561 |
| Congenital Lipomatous Overgrowth, Vascular Malformations, And Epidermal Nevi |
|
Renal hypoplasia, Nephroblastoma, Spinal dysraphism |
OMIM:612918 |
| Lujo Hemorrhagic Fever |
|
Purpura, Ecchymosis, Oliguria, Dysphagia, Renal insufficiency, Microscopic hematuria |
ORPHA:319213 |
| Caudal Regression Syndrome |
|
Vesicoureteral reflux, Arrhinencephaly, Renal agenesis, Ectopic kidney, Abnormality of the ureter... |
ORPHA:3027 |
| Cystinosis |
|
Hypokalemia, Hypophosphatemia, Gait disturbance, Corneal opacity, Polydipsia |
ORPHA:213 |
| Cholera |
|
Palmoplantar cutis laxa, Abnormality of renal excretion, Acute kidney injury, Decreased urine out... |
ORPHA:173 |
| Short-Rib Thoracic Dysplasia 7 With Or Without Polydactyly |
|
Renal cyst, Polycystic kidney dysplasia, Renal hypoplasia, Hypospadias |
OMIM:614091 |
| Prune Belly Syndrome |
|
Urogenital sinus anomaly, Vesicoureteral reflux, Patent ductus arteriosus, Multicystic kidney dys... |
ORPHA:2970 |
| Osteoporosis-Oculocutaneous Hypopigmentation Syndrome |
|
Pallor |
ORPHA:2786 |
| Hypoparathyroidism-Sensorineural Deafness-Renal Disease Syndrome |
|
Vesicoureteral reflux, Renal dysplasia, Polycystic kidney dysplasia, Unilateral renal agenesis, R... |
ORPHA:2237 |
| Hypomagnesemia 3, Renal |
|
Hypocitraturia, Hypercitraturia, Hypermagnesiuria, Recurrent urinary tract infections, Hematuria,... |
OMIM:248250 |
| Paget Disease Of Bone 5, Juvenile-Onset |
|
Hydroxyprolinemia, Hyperuricemia, Hyperphosphatemia |
OMIM:239000 |
| Takenouchi-Kosaki Syndrome |
|
Patent ductus arteriosus, Hypospadias, Unilateral renal agenesis, Hydronephrosis |
OMIM:616737 |
| Neurodevelopmental Disorder With Seizures, Microcephaly, And Brain Abnormalities |
|
Patent ductus arteriosus, Neonatal death, Unilateral renal agenesis |
OMIM:620024 |
| Exstrophy-Epispadias Complex |
|
Vesicoureteral reflux, Urinary incontinence, Bladder exstrophy, Renal duplication, Absent penis, ... |
ORPHA:322 |
| Urofacial Syndrome 1 |
|
Recurrent urinary tract infections, Hydroureter, Enuresis, Urethral valve, Urethral obstruction, ... |
OMIM:236730 |
| Marden-Walker Syndrome |
|
Renal hypoplasia, Hypospadias, Micropenis |
OMIM:248700 |
| Igg4-Related Retroperitoneal Fibrosis |
|
Nephrotic syndrome, Acute kidney injury, Dysuria, Renal tubular epithelial necrosis, Membranous n... |
ORPHA:49041 |
| Schizophrenia 1 |
|
Ectopic kidney, Renal agenesis, Partially duplicated kidney |
OMIM:181510 |
| Drug-Induced Autoimmune Hemolytic Anemia |
|
Abnormal urinary color, Pallor |
ORPHA:90037 |
| Breath-Holding Spells |
|
Pallor |
OMIM:607578 |
| Leber Congenital Amaurosis 14 |
|
Pallor |
OMIM:613341 |
| Cold Agglutinin Disease |
|
Abnormal urinary color, Pallor |
ORPHA:56425 |
| Carnitine-Acylcarnitine Translocase Deficiency |
|
Dicarboxylic aciduria, Oliguria |
ORPHA:159 |
| Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome |
|
Agitation, Pallor |
ORPHA:276608 |
| Hyperinsulinism Due To Ucp2 Deficiency |
|
Polyphagia, Agitation, Pallor |
ORPHA:276556 |
| Hyperparathyroidism, Transient Neonatal |
|
Patent ductus arteriosus, Enlarged kidney, Unilateral renal agenesis, Umbilical hernia |
OMIM:618188 |
| Hemorrhagic Destruction Of The Brain, Subependymal Calcification, And Cataracts |
|
Ectopic kidney, Neonatal death, Cystic renal dysplasia, Death in infancy |
OMIM:613730 |
| Pseudohypoparathyroidism With Albright Hereditary Osteodystrophy |
|
Hyperphosphatemia |
ORPHA:457059 |
| Duane-Radial Ray Syndrome |
|
Vesicoureteral reflux, Crossed fused renal ectopia, Renal malrotation, Renal agenesis, Spina bifi... |
OMIM:607323 |
| Fanconi Anemia, Complementation Group O |
|
Death in infancy, Stage 5 chronic kidney disease, Miscarriage, Renal cyst, Neonatal death, Hydron... |
OMIM:613390 |
| Dystonia, Dopa-Responsive, Due To Sepiapterin Reductase Deficiency |
|
Transient hyperphenylalaninemia, Hyperactivity, Choreoathetosis, Ataxia |
OMIM:612716 |
| Yellow Fever |
|
Acute kidney injury, Renal insufficiency, Anuria |
ORPHA:99829 |
| Congenital Hemidysplasia With Ichthyosiform Erythroderma And Limb Defects |
|
Unilateral renal agenesis, Stillbirth, Erythema, Umbilical hernia, Hydronephrosis |
OMIM:308050 |
| Hypophosphatemic Bone Disease |
|
Hypophosphatemia |
OMIM:146350 |
| Autoimmune Hemolytic Anemia |
|
Abnormal urinary color, Pallor |
ORPHA:98375 |
| Fanconi Anemia, Complementation Group F |
|
Patent ductus arteriosus, Vesicoureteral reflux, Microphallus, Pelvic kidney, Renal hypoplasia |
OMIM:603467 |
| Hypophosphatemic Rickets, Autosomal Dominant |
|
Hypophosphatemia, Hypophosphatemic rickets |
OMIM:193100 |
| Pallister-Hall Syndrome |
|
Patent ductus arteriosus, Renal dysplasia, Hydroureter, Renal cyst, Ectopic kidney, Renal hypopla... |
OMIM:146510 |
| Mitochondrial Complex I Deficiency, Nuclear Type 18 |
|
Hydroureter, Death in infancy, Hydronephrosis |
OMIM:618240 |
| Khan-Khan-Katsanis Syndrome |
|
Vesicoureteral reflux, Patent ductus arteriosus after premature birth, Renal cyst, Dysphagia, Ren... |
OMIM:618460 |
| Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency |
|
Polyphagia, Agitation, Pallor |
ORPHA:276575 |
| Autosomal Dominant Kenny-Caffey Syndrome |
|
Developmental cataract, Hypocalcemic tetany, Hyperphosphatemia, Hypocalcemic seizures |
ORPHA:93325 |
| Aniridia, Microcornea, And Spontaneously Reabsorbed Cataract |
|
Cataract, Aniridia, Microcornea |
OMIM:106230 |
| Fanconi Anemia, Complementation Group L |
|
Renal hypoplasia, Micropenis, Attention deficit hyperactivity disorder, Unilateral renal agenesis |
OMIM:614083 |
| Car T Cell Therapy-Associated Cytokine Release Syndrome |
|
Acute kidney injury, Decreased urine output |
ORPHA:542323 |
| Autosomal Dominant Hyperinsulinism Due To Kir6.2 Deficiency |
|
Polyphagia, Agitation, Pallor |
ORPHA:276580 |
| Mixed-Type Autoimmune Hemolytic Anemia |
|
Abnormal urinary color, Pallor |
ORPHA:90036 |
| Hyperinsulinism Due To Hnf4A Deficiency |
|
Glycosuria, Agitation, Pallor, Proteinuria, Renal Fanconi syndrome |
ORPHA:263455 |
| Acrodysostosis 1 With Or Without Hormone Resistance |
|
Hyperphosphatemia, Blue irides |
OMIM:101800 |
| Neurodevelopmental Disorder With Microcephaly, Cataracts, And Renal Abnormalities |
|
Aminoaciduria, Renal artery stenosis, Dysphagia, Renal hypoplasia, Nephrocalcinosis, Hydronephrosis |
OMIM:617913 |
| Hyperinsulinism Due To Hnf1A Deficiency |
|
Polyphagia, Agitation, Pallor |
ORPHA:324575 |
| Bardet-Biedl Syndrome 17 |
|
Stage 5 chronic kidney disease, Renal cyst, Polyuria, Micropenis, Polydipsia |
OMIM:615994 |
| Acrodysostosis With Multiple Hormone Resistance |
|
Hyperactivity, Hypocalcemia, Blue irides, Hyperphosphatemia |
ORPHA:280651 |
| Mayer-Rokitansky-Küster-Hauser Syndrome Type 2 |
|
Ectopic kidney, Renal agenesis, Renal dysplasia |
ORPHA:2578 |
| Teratoma, Pineal |
|
Polyuria, Polydipsia |
OMIM:273120 |
| Mohr-Tranebjaerg Syndrome |
|
Abnormal posturing, Dysphagia |
OMIM:304700 |
| Intellectual Disability Syndrome Due To A Dyrk1A Point Mutation |
|
Patent ductus arteriosus, Unilateral renal agenesis, Renal cyst, Hypospadias, Attention deficit h... |
ORPHA:464311 |
| Histidinemia |
|
Hyperactivity, Hyperhistidinemia |
ORPHA:2157 |
| Malignant Hyperthermia Of Anesthesia |
|
Hyperphosphatemia, Hyperkalemia, Elevated creatine kinase after exercise |
ORPHA:423 |
| Pseudotrisomy 13 Syndrome |
|
Renal hypoplasia, Renal agenesis, Encephalocele, Micropenis |
OMIM:264480 |
| Hemoglobin D Disease |
|
Pallor |
ORPHA:90039 |
| 7Q11.23 Microduplication Syndrome |
|
Patent ductus arteriosus, Hyperactivity, Unilateral renal agenesis, Hypospadias, Polyphagia, Enur... |
ORPHA:96121 |
| Sporadic Pheochromocytoma/Secreting Paraganglioma |
|
Hematuria, Elevated urinary epinephrine, Glomerular sclerosis, Elevated urinary dopamine, Pallor,... |
ORPHA:276621 |
| Ethylene Glycol Poisoning |
|
Decreased urine output, Renal tubular epithelial necrosis, Hematuria, Renal insufficiency, Alcoho... |
ORPHA:31826 |
| Myoectodermal Gonadal Dysgenesis Syndrome |
|
Scaling skin, Dry skin, Unilateral renal agenesis |
OMIM:618419 |
| Microphthalmia, Syndromic 9 |
|
Patent ductus arteriosus, Renal malrotation, Horseshoe kidney, Pelvic kidney, Renal hypoplasia, H... |
OMIM:601186 |
| Cyclic Vomiting Syndrome |
|
Attention deficit hyperactivity disorder, Pallor |
OMIM:500007 |
| Angelman Syndrome Due To Imprinting Defect In 15Q11-Q13 |
|
Hyperactivity, Iris hypopigmentation, Ataxia, Polyphagia, Broad-based gait |
ORPHA:411515 |
| Acute Myelomonocytic Leukemia |
|
Pallor |
ORPHA:517 |
| Developmental Delay, Language Impairment, And Ocular Abnormalities |
|
Hyperactivity, Developmental cataract, Impulsivity, Attention deficit hyperactivity disorder, Myo... |
OMIM:620141 |
| Optic Atrophy 7 With Or Without Auditory Neuropathy |
|
Pallor |
OMIM:612989 |
| Helix Syndrome |
|
Polyuria, Hypocalciuria, Renal insufficiency, Nephrolithiasis, Dry skin, Polydipsia |
OMIM:617671 |
| Autosomal Dominant Hypocalcemia |
|
Hypocalcemia, Hypomagnesemia, Hyperphosphatemia |
ORPHA:428 |
| Childhood Absence Epilepsy |
|
Urinary incontinence, Attention deficit hyperactivity disorder, Pallor |
ORPHA:64280 |
| Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia |
|
Hyperactivity, Attention deficit hyperactivity disorder |
OMIM:617182 |
| Dyrk1A-Related Intellectual Disability Syndrome |
|
Patent ductus arteriosus, Hyperactivity, Unilateral renal agenesis, Renal cyst, Hypospadias, Pelv... |
ORPHA:464306 |
| Renal Tubulopathy, Diabetes Mellitus, And Cerebellar Ataxia |
|
Proximal tubulopathy, Polyuria, Death in childhood, Death in adolescence |
OMIM:560000 |
| Combined Immunodeficiency With Faciooculoskeletal Anomalies |
|
Unilateral renal agenesis, Umbilical hernia, Recurrent urinary tract infections |
ORPHA:221139 |
| Caudal Duplication |
|
Myelomeningocele, Renal hypoplasia/aplasia, Spina bifida, Ureteral duplication, Abnormal penis mo... |
ORPHA:1756 |
| Rheumatic Fever |
|
Pallor, Erythema, Nephrotic syndrome |
ORPHA:3099 |
| Cataract 10, Multiple Types |
|
Posterior Y-sutural cataract, Nuclear cataract, Zonular cataract, Developmental cataract |
OMIM:600881 |
| Diabetes Insipidus, Nephrogenic, 2, Autosomal |
|
Polyuria, Polydipsia, Megacystis |
OMIM:125800 |
| Diabetes Insipidus, Nephrogenic, 1, X-Linked |
|
Polyuria, Polydipsia, Megacystis |
OMIM:304800 |
| Hereditary Hypophosphatemic Rickets With Hypercalciuria |
|
Hypophosphatemia, Hypophosphatemic rickets, Increased circulating beta-C-terminal telopeptide con... |
ORPHA:157215 |
| Amelogenesis Imperfecta, Type Ig |
|
Impaired renal concentrating ability, Nephrocalcinosis, Polyuria, Enuresis, Renal insufficiency |
OMIM:204690 |
| Familial Focal Epilepsy With Variable Foci |
|
Pallor |
ORPHA:98820 |
| Congenital Myopathy 17 |
|
Renal hypoplasia, Ureteropelvic junction obstruction, Hydronephrosis |
OMIM:618975 |
| Short-Rib Thoracic Dysplasia 13 With Or Without Polydactyly |
|
Patent ductus arteriosus, Encephalocele, Renal cyst, Stillbirth, Renal hypoplasia |
OMIM:616300 |
| Dent Disease 2 |
|
Hypophosphatemia, Elevated circulating creatine kinase concentration |
OMIM:300555 |
| Primary Hyperoxaluria Type 2 |
|
Renal insufficiency, Recurrent urinary tract infections, Nephrocalcinosis, Ureteral obstruction, ... |
ORPHA:93599 |
| X-Linked Sideroblastic Anemia |
|
Pallor |
ORPHA:75563 |
| Idiopathic Pulmonary Hemosiderosis |
|
Glomerulonephritis, Pallor |
ORPHA:99931 |
| Autosomal Recessive Polycystic Kidney Disease |
|
Recurrent urinary tract infections, Acute kidney injury, Enlarged kidney, Polycystic kidney dyspl... |
ORPHA:731 |
| Microphthalmia-Microtia-Fetal Akinesia Syndrome |
|
Patent ductus arteriosus, Hydroureter, Abnormality of the upper urinary tract, Hypoplasia of peni... |
ORPHA:2547 |
| Cockayne Syndrome Type 3 |
|
Urinary retention, Neurogenic bladder, Hydroureter, Unilateral renal agenesis, Renal hypoplasia, ... |
ORPHA:90324 |
| Sporadic Infantile Bilateral Striatal Necrosis |
|
Urinary incontinence, Abnormal posturing, Titubation, Dysphagia |
ORPHA:225147 |
| Neurofaciodigitorenal Syndrome |
|
Unilateral renal agenesis |
ORPHA:2673 |
| Autosomal Dominant Cutis Laxa |
|
Cutis laxa, Dermal translucency, Premature skin wrinkling, Bladder diverticulum, Pyelonephritis, ... |
ORPHA:90348 |
| Distal 16P11.2 Microdeletion Syndrome |
|
Vesicoureteral reflux, Abnormality of the kidney, Renal agenesis, Attention deficit hyperactivity... |
ORPHA:261222 |
| Colchicine Poisoning |
|
Renal insufficiency, Oliguria |
ORPHA:31824 |
| Juvenile Huntington Disease |
|
Gait ataxia, Hyperactivity, Ataxia, Progressive cerebellar ataxia, Broad-based gait |
ORPHA:248111 |
| Methylmalonic Aciduria And Homocystinuria, Cblj Type |
|
Patent ductus arteriosus, Methylmalonic aciduria, Homocystinuria, Abnormal posturing |
OMIM:614857 |
| Phakomatosis Pigmentokeratotica |
|
Nephroblastoma, Unilateral renal hypoplasia, Spina bifida, Renal transitional cell carcinoma |
ORPHA:2874 |
| Guanidinoacetate Methyltransferase Deficiency |
|
Hyperactivity, Athetosis, Ataxia |
ORPHA:382 |
| Scalp-Ear-Nipple Syndrome |
|
Pyelonephritis, Unilateral renal agenesis, Renal hypoplasia, Renal insufficiency, Dry skin |
OMIM:181270 |
| Autoimmune Hemolytic Anemia, Warm Type |
|
Abnormal urinary color, Pallor |
ORPHA:90033 |
| Andersen-Tawil Syndrome |
|
Renal hypoplasia, Renal tubular dysfunction |
ORPHA:37553 |
| Developmental Delay With Or Without Dysmorphic Facies And Autism |
|
Patent ductus arteriosus, Vesicoureteral reflux, Microphallus, Renal cyst, Renal hypoplasia, Umbi... |
OMIM:618454 |
| Anterior Segment Dysgenesis 7 |
|
Ocular anterior segment dysgenesis, Anterior synechiae of the anterior chamber, Microcornea, Buph... |
OMIM:269400 |
| Ureter, Bifid Or Double |
|
Ureteral duplication |
OMIM:191550 |
| Chromosome 19Q13.11 Deletion Syndrome, Proximal |
|
Vesicoureteral reflux, Hydroureter, Nephrolithiasis |
OMIM:617219 |
| Caudal Duplication Anomaly |
|
Ureteral duplication |
OMIM:607864 |
| Ureterocele |
|
Duplicated collecting system, Ureterocele |
OMIM:191650 |
| Short-Rib Thoracic Dysplasia 12 |
|
Patent ductus arteriosus, Anencephaly, Cystic renal dysplasia, Renal hypoplasia, Neonatal death |
OMIM:269860 |
| Aneurysm Of Sinus Of Valsalva |
|
Oliguria |
ORPHA:1054 |
| Neurofacioskeletal Syndrome With Or Without Renal Agenesis |
|
Hydroureter, Unilateral renal agenesis, Bilateral renal agenesis |
OMIM:619194 |
| Fanconi Renotubular Syndrome 5 |
|
Hypophosphatemia, Hypophosphatemic rickets |
OMIM:618913 |
| Penile Agenesis |
|
Absent penis, Bilateral renal agenesis, Urethral fistula, Hydroureter, Cystic renal dysplasia, Ab... |
ORPHA:49 |
| Microcephaly-Corpus Callosum Hypoplasia-Intellectual Disability-Facial Dysmorphism Syndrome |
|
Hyperactivity, Unilateral renal agenesis |
ORPHA:457284 |
| Stromme Syndrome |
|
Stillbirth, Bilateral renal hypoplasia, Hydronephrosis |
OMIM:243605 |
| Intellectual Developmental Disorder, Autosomal Recessive 38 |
|
Unsteady gait, Blue irides, Hyperactivity |
OMIM:615516 |
| Bladder Exstrophy |
|
Vesicoureteral reflux, Recurrent urinary tract infections, Hypoplasia of penis, Epispadias, Abnor... |
ORPHA:93930 |
| Cerebrofacioarticular Syndrome |
|
Renal hypoplasia, Hypospadias |
ORPHA:314679 |
| Nephrolithiasis/Osteoporosis, Hypophosphatemic, 2 |
|
Hypophosphatemia |
OMIM:612287 |
| Van Maldergem Syndrome 1 |
|
Renal hypoplasia, Hypospadias |
OMIM:601390 |
| Bartter Syndrome, Type 4A, Neonatal, With Sensorineural Deafness |
|
Impaired renal concentrating ability, Renal salt wasting, Hypernatriuria, Hyperchloriduria, Reduc... |
OMIM:602522 |
| Smith-Lemli-Opitz Syndrome |
|
Patent ductus arteriosus, Hyperactivity, Death in infancy, Renal agenesis, Unilateral renal agene... |
OMIM:270400 |
| Hereditary Pheochromocytoma-Paraganglioma |
|
Renal cell carcinoma, Hematuria, Elevated urinary epinephrine, Glomerular sclerosis, Elevated uri... |
ORPHA:29072 |
| Silver-Russell Syndrome 1 |
|
Nephroblastoma, Congenital posterior urethral valve, Abnormality of the ureter, Hypospadias, Uret... |
OMIM:180860 |
| Microcephalic Cortical Malformations-Short Stature Due To Rttn Deficiency |
|
Microphallus, Unilateral renal agenesis, Hypospadias, Pelvic kidney, Abnormal renal collecting sy... |
ORPHA:468631 |
| Craniofacial Dysmorphism, Skeletal Anomalies, And Impaired Intellectual Development Syndrome 1 |
|
Patent ductus arteriosus, Attention deficit hyperactivity disorder, Unilateral renal agenesis |
OMIM:213980 |
| Xy Type Gonadal Dysgenesis-Associated Anomalies Syndrome |
|
Renal hypoplasia/aplasia, Abnormality of the ureter, Umbilical hernia |
ORPHA:1770 |
| Distal 22Q11.2 Microduplication Syndrome |
|
Patent ductus arteriosus, Attention deficit hyperactivity disorder, Branchial fistula, Unilateral... |
ORPHA:261337 |
| Spontaneous Periodic Hypothermia |
|
Pallor |
ORPHA:29822 |
| 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency |
|
Dysphagia, Restlessness, Agitation, Pallor |
ORPHA:13 |
| Microcephaly-Cervical Spine Fusion Anomalies Syndrome |
|
Abnormality of the ureter, Hypospadias |
ORPHA:2522 |
| Ifap Syndrome 1, With Or Without Bresheck Syndrome |
|
Perianal erythema, Multicystic kidney dysplasia, Renal dysplasia, Death in infancy, Renal agenesi... |
OMIM:308205 |
| Bartter Syndrome, Type 5, Antenatal, Transient |
|
Polyuria, Medullary nephrocalcinosis, Hypercalciuria |
OMIM:300971 |
| Bartter Syndrome, Type 3 |
|
Renal salt wasting, Hyperchloriduria, Increased urinary potassium, Polyuria, Hypocalciuria, Impai... |
OMIM:607364 |
| Ventriculomegaly With Defects Of The Radius And Kidney |
|
Ectopic kidney, Renal agenesis, Horseshoe kidney, Ureteral duplication |
OMIM:602200 |
| Van Maldergem Syndrome 2 |
|
Renal hypoplasia, Hypospadias, Micropenis |
OMIM:615546 |
| Cornelia De Lange Syndrome 1 |
|
Vesicoureteral reflux, Renal cyst, Reduced renal corticomedullary differentiation, Hypospadias, E... |
OMIM:122470 |
| Juvenile Nephropathic Cystinosis |
|
Hypocalcemic tetany, Hypophosphatemia, Hypokalemia, Corneal crystals, Abnormal cornea morphology,... |
ORPHA:411634 |
| Infantile Nephropathic Cystinosis |
|
Hypokalemia, Hypophosphatemia, Corneal crystals, Abnormal blood ion concentration, Abnormal corne... |
ORPHA:411629 |
| Familial Isolated Hyperparathyroidism |
|
Hypophosphatemia, Hypercalcemia |
ORPHA:99879 |
| Congenital Adrenal Hyperplasia Due To Cytochrome P450 Oxidoreductase Deficiency |
|
Vesicoureteral reflux, Unilateral renal agenesis, Hypospadias, Stillbirth, Dilatation of the rena... |
ORPHA:95699 |
| Exercise-Induced Malignant Hyperthermia |
|
Hyperphosphatemia, Hyperkalemia, Ataxia, Elevated circulating creatine kinase concentration, Hypo... |
ORPHA:466650 |
| Ectopia Lentis Et Pupillae |
|
Iris transillumination defect, Ectopia lentis, Cataract, Ectopia pupillae, Persistent pupillary m... |
OMIM:225200 |
| Vitamin D Hydroxylation-Deficient Rickets, Type 1B |
|
Hypophosphatemia, Hypocalcemia, Difficulty walking |
OMIM:600081 |
| Urban-Rogers-Meyer Syndrome |
|
Abnormality of the ureter, Hypoplasia of penis |
ORPHA:3409 |
| Cardiogenic Shock |
|
Oliguria |
ORPHA:97292 |
| Fanconi Anemia, Complementation Group A |
|
Renal agenesis, Ectopic kidney, Duplicated collecting system, Horseshoe kidney, Anemic pallor, Ab... |
OMIM:227650 |
| Hyperparathyroidism, Neonatal Severe |
|
Hypophosphatemia, Hypercalcemia, Polydipsia, Calcinosis |
OMIM:239200 |
| Beta-Ketothiolase Deficiency |
|
Oral aversion, Pallor, Agitation, Ketonuria |
ORPHA:134 |
| Hypophosphatemic Rickets With Hypercalciuria, Hereditary |
|
Abnormal circulating calcium concentration, Hypophosphatemia, Hypophosphatemic rickets, Difficult... |
OMIM:241530 |
| Leopard Syndrome 1 |
|
Spina bifida occulta, Micropenis, Hypospadias, Unilateral renal agenesis |
OMIM:151100 |
| Ulnar-Mammary Syndrome |
|
Renal hypoplasia, Hypoplasia of penis |
ORPHA:3138 |
| Hyperaldosteronism, Familial, Type Iii |
|
Polyuria, Hypercalciuria, Polydipsia |
OMIM:613677 |
| Axial Mesodermal Dysplasia Spectrum |
|
Renal hypoplasia/aplasia, Renal cyst, Abnormality of the ureter, Abnormal localization of kidney,... |
ORPHA:1834 |
| Autosomal Dominant Hypophosphatemic Rickets |
|
Hypophosphatemia, Hypocalcemia |
ORPHA:89937 |
| Nephrolithiasis/Osteoporosis, Hypophosphatemic, 1 |
|
Hypophosphatemia |
OMIM:612286 |
| Macrothrombocytopenia-Lymphedema-Developmental Delay-Facial Dysmorphism-Camptodactyly Syndrome |
|
Patent ductus arteriosus, Hypospadias, Unilateral renal agenesis, Hydronephrosis |
ORPHA:487796 |
| Kinsship Syndrome |
|
Renal hypoplasia, Horseshoe kidney, Death in infancy |
OMIM:619297 |
| Cockayne Syndrome |
|
Urinary incontinence, Nephrotic syndrome, Neurogenic bladder, Premature skin wrinkling, Unilatera... |
ORPHA:191 |
| Fanconi Anemia, Complementation Group E |
|
Renal agenesis, Ectopic kidney, Duplicated collecting system, Horseshoe kidney, Anemic pallor |
OMIM:600901 |
| Hyperuricemia, Pulmonary Hypertension, Renal Failure, And Alkalosis Syndrome |
|
Renal salt wasting, Polyuria, Proteinuria, Hyperechogenic kidneys, Chronic kidney disease |
OMIM:613845 |
| Thiamine-Responsive Megaloblastic Anemia Syndrome |
|
Pallor |
ORPHA:49827 |
| Dravet Syndrome |
|
Impulsivity, Pallor |
ORPHA:33069 |
| Refractory Celiac Disease |
|
Hypophosphatemia, Hypoproteinemia, Hypocalcemia, Hypomagnesemia, Hypoalbuminemia |
ORPHA:398063 |
| Alagille Syndrome 1 |
|
Vesicoureteral reflux, Multiple small medullary renal cysts, Renal tubular acidosis, Renal dyspla... |
OMIM:118450 |
| Arima Syndrome |
|
Renal tubular atrophy, Stage 5 chronic kidney disease, Renal sodium wasting, Polycystic kidney dy... |
OMIM:243910 |
| Hypophosphatemic Rickets And Hyperparathyroidism |
|
Hypophosphatemia, Hypophosphatemic rickets, Hypercalcemia |
OMIM:612089 |
| Seizures, Sensorineural Deafness, Ataxia, Impaired Intellectual Development, And Electrolyte Imbalance |
|
Renal sodium wasting, Renal salt wasting, Polyuria, Hypocalciuria, Salt craving, Enuresis, Polydi... |
OMIM:612780 |
| Proteinuria, Low Molecular Weight, With Hypercalciuria And Nephrocalcinosis |
|
Hypophosphatemia |
OMIM:308990 |
| Zttk Syndrome |
|
Patent ductus arteriosus, Horseshoe kidney, Polyuria, Unilateral renal agenesis |
OMIM:617140 |
| Syndromic Diarrhea |
|
Renal hypoplasia, Polycystic kidney dysplasia, Dry skin, Patent ductus arteriosus |
ORPHA:84064 |
| Hereditary Orotic Aciduria |
|
Patent ductus arteriosus, Aminoaciduria, Oroticaciduria, Abnormality of the ureter, Orotic acid c... |
ORPHA:30 |
| Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 3 |
|
Hydroureter, Megacystis, Neonatal death, Fetal megacystis, Hydronephrosis |
OMIM:619362 |
| Vitamin D Hydroxylation-Deficient Rickets, Type 1A |
|
Hypophosphatemia, Hypocalcemia, Difficulty walking, Hypocalcemic seizures |
OMIM:264700 |
| Beta-Thalassemia Intermedia |
|
Proximal tubulopathy, Skin ulcer, Pallor |
ORPHA:231222 |
| Poland Syndrome |
|
Vesicoureteral reflux, Encephalocele, Renal hypoplasia/aplasia, Spina bifida occulta, Hypospadias... |
ORPHA:2911 |
| Hypocalcemic Vitamin D-Resistant Rickets |
|
Gait disturbance, Hypophosphatemia, Hypocalcemia |
ORPHA:93160 |
| Huntington Disease-Like 1 |
|
Abnormal posturing, Restlessness |
ORPHA:157941 |
| Trisomy 13 |
|
Patent ductus arteriosus, Abnormality of the ureter, Multiple renal cysts, Displacement of the ur... |
ORPHA:3378 |
| Dyrk1A-Related Intellectual Disability Syndrome Due To 21Q22.13Q22.2 Microdeletion |
|
Recurrent urinary tract infections, Unilateral renal agenesis, Hypospadias, Dilatation of the ren... |
ORPHA:268261 |
| Intellectual Disability-Cardiac Anomalies-Short Stature-Joint Laxity Syndrome |
|
Spina bifida, Renal agenesis, Hypospadias, Horseshoe kidney, Pelvic kidney, Renal hypoplasia |
ORPHA:508498 |
| 8Q24.3 Microdeletion Syndrome |
|
Patent ductus arteriosus, Vesicoureteral reflux, Hyperactivity, Abnormality of the kidney, Unilat... |
ORPHA:508488 |
| Alport Syndrome 3, Autosomal Dominant |
|
Azotemia, Anterior polar cataract, Hypophosphatemia, Lenticonus |
OMIM:104200 |
| Plummer-Vinson Syndrome |
|
Dysphagia, Geophagia, Pallor |
ORPHA:54028 |
| Classic Pantothenate Kinase-Associated Neurodegeneration |
|
Abnormal posturing, Attention deficit hyperactivity disorder, Dysphagia |
ORPHA:216866 |
| Degcags Syndrome |
|
Patent ductus arteriosus, Abnormal renal cortex morphology, Abnormal renal medulla morphology, Re... |
OMIM:619488 |
| Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 1 |
|
Hydroureter, Fetal megacystis |
OMIM:249210 |
| Myopathic Ehlers-Danlos Syndrome |
|
Pallor |
ORPHA:536516 |
| Fanconi Anemia, Complementation Group D2 |
|
Patent ductus arteriosus, Renal duplication, Renal agenesis, Ectopic kidney, Duplicated collectin... |
OMIM:227646 |
| Prune Belly Syndrome |
|
Congenital posterior urethral valve, Hydroureter, Patent ductus arteriosus, Hydronephrosis |
OMIM:100100 |
| Fumarase Deficiency |
|
Aminoaciduria, Pallor |
OMIM:606812 |
| Anemia, Congenital Dyserythropoietic, Type Ib |
|
Pallor |
OMIM:615631 |
| Cataract 5, Multiple Types |
|
Lamellar cataract, Zonular cataract, Pulverulent cataract, Anterior polar cataract, Nuclear cataract |
OMIM:116800 |
| Evans Syndrome |
|
Petechiae, Pallor |
ORPHA:1959 |
| Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema |
|
Hemoglobinuria, Pallor |
OMIM:194380 |
| Leishmaniasis |
|
Skin ulcer, Pallor |
ORPHA:507 |
| Fructose-1,6-Bisphosphatase Deficiency |
|
Pallor, Increased urinary glycerol |
ORPHA:348 |
| Diamond-Blackfan Anemia 1 |
|
Renal hypoplasia, Pallor |
OMIM:105650 |
| Acrofacial Dysostosis 1, Nager Type |
|
Patent ductus arteriosus, Unilateral renal agenesis |
OMIM:154400 |
| 22Q11.2 Deletion Syndrome |
|
Meningocele, Vesicoureteral reflux, Patent ductus arteriosus, Spina bifida, Polycystic kidney dys... |
ORPHA:567 |
| Fanconi Renotubular Syndrome 1 |
|
Hypokalemia, Hypophosphatemia |
OMIM:134600 |
| Aredyld Syndrome |
|
Abnormality of the ureter |
ORPHA:1133 |
| Waldenström Macroglobulinemia |
|
Renal insufficiency, Purpura, Pallor |
ORPHA:33226 |
| Beta-Thalassemia |
|
Skin ulcer, Pallor |
ORPHA:848 |
| Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease |
|
Multiple small medullary renal cysts, Neonatal death, Enlarged kidney, Polycystic kidney dysplasi... |
OMIM:263200 |
| Proboscis Lateralis |
|
Ureteral agenesis, Duplication of renal pelvis, Unilateral renal agenesis, Patent ductus arteriosus |
ORPHA:141099 |
| Cloacal Exstrophy |
|
Vesicoureteral reflux, Myelomeningocele, Renal hypoplasia/aplasia, Hydroureter, Spina bifida, Hyp... |
ORPHA:93929 |
| Bartter Syndrome, Type 4B, Neonatal, With Sensorineural Deafness |
|
Renal salt wasting, Hypernatriuria, Hyperchloriduria, Increased urinary potassium, Polyuria, Decr... |
OMIM:613090 |
| Anemia, Nonspherocytic Hemolytic, Due To G6Pd Deficiency |
|
Hemoglobinuria, Pallor |
OMIM:300908 |
| Oncogenic Osteomalacia |
|
Gait disturbance, Hypophosphatemia, Hypocalcemia |
ORPHA:352540 |
| Vitamin D-Dependent Rickets, Type 2A |
|
Hypophosphatemia, Difficulty walking, Hypocalcemic seizures |
OMIM:277440 |
| Hereditary Fructose Intolerance |
|
Hypophosphatemia, Hyperuricemia, Cataract, Hypermagnesemia |
ORPHA:469 |
| Fanconi Anemia, Complementation Group C |
|
Renal agenesis, Ectopic kidney, Duplicated collecting system, Horseshoe kidney, Anemic pallor |
OMIM:227645 |
| Panhypophysitis |
|
Hyposthenuria, Polydipsia, Pallor |
ORPHA:95513 |
| Nephrogenic Diabetes Insipidus |
|
Hyposthenuria, Enuresis nocturna, Hydroureter, Renal insufficiency, Functional abnormality of the... |
ORPHA:223 |
| Metaphyseal Chondrodysplasia, Jansen Type |
|
Hypophosphatemia, Hypercalcemia, Waddling gait |
OMIM:156400 |
| Atresia Of Urethra |
|
Vesicoureteral reflux, Recurrent urinary tract infections, Renal dysplasia, Hydroureter, Bladder ... |
ORPHA:105 |
| Fanconi-Bickel Syndrome |
|
Hypokalemia, Hypophosphatemia, Hypouricemia |
OMIM:227810 |
| Gitelman Syndrome |
|
Nocturia, Polyuria, Hypocalciuria, Salt craving, Renal magnesium wasting, Enuresis, Polydipsia, R... |
OMIM:263800 |
| Hypophosphatemic Rickets, X-Linked Dominant |
|
Abnormal circulating calcium concentration, Hypophosphatemia, Hypophosphatemic rickets |
OMIM:307800 |
| Smith-Magenis Syndrome |
|
Renal hypoplasia/aplasia, Abnormality of the ureter, Attention deficit hyperactivity disorder, Ab... |
ORPHA:819 |
| Uremic Pruritus |
|
Increased blood urea nitrogen, Renal hypophosphatemia, Hypercalcemia, Hypermagnesemia |
ORPHA:94059 |
| Autosomal Recessive Spondylocostal Dysostosis |
|
Meningocele, Spina bifida occulta, Abnormality of the ureter, Hypospadias, Umbilical hernia |
ORPHA:2311 |
| Serkal Syndrome |
|
Hypospadias, Hypoplasia of the bladder, Renal agenesis, Abnormal penis morphology |
ORPHA:139466 |
| Primary Myelofibrosis |
|
Ecchymosis, Purpura, Petechiae, Pallor |
ORPHA:824 |
| Cataract 20, Multiple Types |
|
Cortical cataract, Sutural cataract, Lamellar cataract, Membranous cataract |
OMIM:116100 |
| 14Q22Q23 Microdeletion Syndrome |
|
Renal hypoplasia |
ORPHA:264200 |
| Pearson Marrow-Pancreas Syndrome |
|
Pallor, Complex organic aciduria, Erythema, 3-Methylglutaric aciduria, Renal Fanconi syndrome, De... |
OMIM:557000 |
| Insensitivity To Pain, Congenital, With Anhidrosis |
|
Hyperactivity, Corneal scarring, Keratitis, Opacification of the corneal stroma, Recurrent cornea... |
OMIM:256800 |
| Imerslund-Gräsbeck Syndrome |
|
Proteinuria, Pallor |
ORPHA:35858 |
| Peutz-Jeghers Syndrome |
|
Renal cell carcinoma, Abnormality of the ureter, Multiple renal cysts |
ORPHA:2869 |
| Hypocalcemic Vitamin D-Dependent Rickets |
|
Hypophosphatemia, Hypocalcemia, Difficulty walking, Hypocalcemic seizures |
ORPHA:289157 |
| Hb Bart'S Hydrops Fetalis |
|
Pallor |
ORPHA:163596 |
| Heterotaxy, Visceral, 5, Autosomal |
|
Renal hypoplasia, Ureteral stenosis, Ureteral duplication, Patent ductus arteriosus |
OMIM:270100 |
| Primordial Dwarfism-Immunodeficiency-Lipodystrophy Syndrome |
|
Renal hypoplasia, Patent ductus arteriosus |
OMIM:620005 |
| Neurodevelopmental Disorder With Hypotonia And Dysmorphic Facies |
|
Facial erythema, Cutis laxa, Urinary urgency, Unilateral renal agenesis, Scaling skin, Impulsivit... |
OMIM:619503 |
| Kcnq2-Related Epileptic Encephalopathy |
|
Facial erythema, Pallor |
ORPHA:439218 |
| Combined Oxidative Phosphorylation Deficiency 55 |
|
Hypophosphatemia, Mildly elevated creatine kinase, Elevated circulating creatine kinase concentra... |
OMIM:619743 |
| Hereditary Folate Malabsorption |
|
Pallor, Recurrent urinary tract infections |
ORPHA:90045 |
| Alagille Syndrome |
|
Renal hypoplasia/aplasia, Spina bifida occulta, Abnormality of the ureter, Nephrotic syndrome |
ORPHA:52 |
| Adenohypophysitis |
|
Hyposthenuria, Pallor |
ORPHA:95512 |
| Digeorge Syndrome |
|
Patent ductus arteriosus, Renal dysplasia, Unilateral renal agenesis, Attention deficit hyperacti... |
OMIM:188400 |
| Myelofibrosis |
|
Purpura, Pallor |
OMIM:254450 |
| Williams-Beuren Syndrome |
|
Umbilical hernia, Vesicoureteral reflux, Cutis laxa, Recurrent urinary tract infections, Nephroca... |
OMIM:194050 |
| Megaloblastic Anemia Due To Dihydrofolate Reductase Deficiency |
|
Pallor |
OMIM:613839 |
| Williams Syndrome |
|
Abnormality of the bladder, Spina bifida occulta, Nephrolithiasis, Vesicoureteral reflux, Hypopla... |
ORPHA:904 |
| 46,Xx Disorder Of Sex Development-Anorectal Anomalies Syndrome |
|
Urogenital sinus anomaly, Multicystic kidney dysplasia, Renal hypoplasia/aplasia, Hydroureter, Ab... |
ORPHA:2973 |
| Irida Syndrome |
|
Pallor |
ORPHA:209981 |
| Cystinosis, Nephropathic |
|
Aminoaciduria, Stage 5 chronic kidney disease, Glycosuria, Hyperphosphaturia, Hematuria, Medullar... |
OMIM:219800 |
| Microcephalic Osteodysplastic Primordial Dwarfism, Type I |
|
Death in infancy, Polycystic kidney dysplasia, Renal cyst, Micropenis, Stillbirth, Renal hypoplas... |
OMIM:210710 |
| Trisomy 20P |
|
Spina bifida, Abnormality of the kidney, Abnormality of the ureter, Hypospadias, Multiple renal c... |
ORPHA:261318 |
| Fraser Syndrome |
|
Urethral atresia, Multicystic kidney dysplasia, Encephalocele, Myelomeningocele, Death in infancy... |
ORPHA:2052 |
| Deafness-Lymphedema-Leukemia Syndrome |
|
Pallor |
ORPHA:3226 |
| Hypocalciuric Hypercalcemia, Familial, Type Iii |
|
Hypophosphatemia, Hypercalcemia, Hypermagnesemia |
OMIM:600740 |
| Myopathy, Lactic Acidosis, And Sideroblastic Anemia 1 |
|
Pallor |
OMIM:600462 |
| Acquired Idiopathic Sideroblastic Anemia |
|
Pallor |
ORPHA:75564 |
| 3-Hydroxy-3-Methylglutaric Aciduria |
|
Pallor, 3-Methylglutaric aciduria, Ketonuria |
ORPHA:20 |
| Fanconi Renotubular Syndrome 4 With Maturity-Onset Diabetes Of The Young |
|
Hypophosphatemia, Hypouricemia |
OMIM:616026 |
| Brain Malformations-Musculoskeletal Abnormalities-Facial Dysmorphism-Intellectual Disability Syndrome |
|
Patent ductus arteriosus after birth at term, Unilateral renal agenesis, Bilateral renal dysplasi... |
ORPHA:500150 |
| Fanconi Renotubular Syndrome 2 |
|
Hypophosphatemia |
OMIM:613388 |
| Hypophosphatemic Rickets, X-Linked Recessive |
|
Hypophosphatemia, Hypophosphatemic rickets |
OMIM:300554 |
| Multiple Endocrine Neoplasia Type 2 |
|
Elevated urinary catecholamines, Elevated urinary vanillylmandelic acid, Elevated urinary epineph... |
ORPHA:653 |
| Renpenning Syndrome 1 |
|
Renal hypoplasia, Phimosis, Hypospadias, Death in childhood |
OMIM:309500 |
| Growth Restriction, Hypoplastic Kidneys, Alopecia, And Distinctive Facies |
|
Renal hypoplasia, Micropenis |
OMIM:619321 |
| Hnf1B-Related Autosomal Dominant Tubulointerstitial Kidney Disease |
|
Glomerulopathy, Multicystic kidney dysplasia, Acute kidney injury, Renal cell carcinoma, Renal ag... |
ORPHA:93111 |
| Short Stature, Brachydactyly, Impaired Intellectual Development, And Seizures |
|
Renal hypoplasia, Redundant neck skin, Recurrent urinary tract infections |
OMIM:617157 |
| Denys-Drash Syndrome |
|
Nephroblastoma, Neonatal death, Nephrotic syndrome, Stage 5 chronic kidney disease, Enlarged kidn... |
OMIM:194080 |
| Lacrimoauriculodentodigital Syndrome |
|
Patent ductus arteriosus, Vesicoureteral reflux, Dysphagia, Renal hypoplasia, Hydronephrosis |
ORPHA:2363 |
| Tessadori-Bicknell-Van Haaften Neurodevelopmental Syndrome 3 |
|
Agitation, Impulsivity, Attention deficit hyperactivity disorder, Unilateral renal hypoplasia, Ex... |
OMIM:619950 |
| Dystonia 1, Torsion, Autosomal Dominant |
|
Abnormal posturing, Dysphagia |
OMIM:128100 |
| Esophageal Atresia |
|
Oral aversion, Renal agenesis, Pallor, Dysphagia, Abnormality of the urinary system |
ORPHA:1199 |
| Pallister-Hall Syndrome |
|
Patent ductus arteriosus, Renal dysplasia, Bilateral renal agenesis, Arrhinencephaly, Unilateral ... |
ORPHA:672 |
| Fraser Syndrome 1 |
|
Encephalocele, Myelomeningocele, Renal hypoplasia/aplasia, Hypospadias, Renal hypoplasia, Micropenis |
OMIM:219000 |
| Sheehan Syndrome |
|
Hyposthenuria, Dry skin, Pallor |
ORPHA:91355 |
| Lumbar Syndrome |
|
Vesicoureteral reflux, Renal duplication, Myelomeningocele, Spina bifida, Renal agenesis, Hypospa... |
ORPHA:83628 |
| Townes-Brocks Syndrome |
|
Patent ductus arteriosus, Vesicoureteral reflux, Urethral valve, Abnormality of the kidney, Hypop... |
ORPHA:857 |
| 17Q12 Microdeletion Syndrome |
|
Renal hypoplasia/aplasia, Renal insufficiency, Multicystic kidney dysplasia, Ureterocele |
ORPHA:261265 |
| Anemia, Hypochromic Microcytic, With Iron Overload 2 |
|
Pallor |
OMIM:615234 |
| Retinitis Pigmentosa 75 |
|
Pallor |
OMIM:617023 |
| Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome |
|
Multicystic kidney dysplasia, Death in infancy, Hydroureter, Megacystis, Umbilical hernia |
ORPHA:2241 |
| Coffin-Siris Syndrome 1 |
|
Patent ductus arteriosus, Hydroureter, Ectopic kidney, Spina bifida occulta, Hypospadias, Renal h... |
OMIM:135900 |
| Pearson Syndrome |
|
Hyperalaninemia, Hypokalemia, Hypophosphatemia, Corneal stromal edema, Ataxia, Cataract, Dysphagi... |
ORPHA:699 |
| Bartter Syndrome, Type 2, Antenatal |
|
Hyposthenuria, Hyperprostaglandinuria, Renal salt wasting, Hyperchloriduria, Increased urinary po... |
OMIM:241200 |
| Von Hippel-Lindau Disease |
|
Renal cell carcinoma, Elevated urinary catecholamines, Multiple renal cysts, Pallor |
ORPHA:892 |
| American Trypanosomiasis |
|
Pallor |
ORPHA:3386 |
| Histiocytoid Cardiomyopathy |
|
Renal cyst, Pallor |
ORPHA:137675 |
| Okamoto Syndrome |
|
Urinary incontinence, Redundant neck skin, Ureteropelvic junction obstruction, Unilateral renal h... |
ORPHA:2729 |
| Anemia, Sideroblastic, 1 |
|
Anemic pallor |
OMIM:300751 |
| Citrullinemia Type Ii |
|
Hyperactivity, Acute hyperammonemia, Hypoproteinemia, Decreased HDL cholesterol concentration, Hy... |
ORPHA:247585 |
| Diarrhea 3, Secretory Sodium, Congenital, With Or Without Other Congenital Anomalies |
|
Ureteral duplication, Cutis laxa |
OMIM:270420 |
| Baller-Gerold Syndrome |
|
Vesicoureteral reflux, Abnormality of the ureter, Abnormal localization of kidney, Hydronephrosis |
ORPHA:1225 |
| Townes-Brocks Syndrome 1 |
|
Vesicoureteral reflux, Multicystic kidney dysplasia, Urethral valve, Renal dysplasia, Hypospadias... |
OMIM:107480 |
| Toriello-Lacassie-Droste Syndrome |
|
Epispadias, Abnormality of the bladder, Abnormality of the ureter, Hypospadias, Abnormal penis mo... |
ORPHA:3339 |
| Fanconi-Bickel Syndrome |
|
Hypophosphatemia, Hypertriglyceridemia |
ORPHA:2088 |
| Fraser Syndrome 3 |
|
Ureteral agenesis, Hypoplasia of the bladder, Bilateral renal agenesis, Hypoplasia of penis, Stil... |
OMIM:617667 |
| Bartter Syndrome, Type 1, Antenatal |
|
Hyposthenuria, Hyperprostaglandinuria, Renal salt wasting, Hyperchloriduria, Increased urinary po... |
OMIM:601678 |
| Junctional Epidermolysis Bullosa With Pyloric Atresia |
|
Renal duplication, Renal dysplasia, Hematuria, Urethral stricture, Urinary bladder inflammation, ... |
ORPHA:79403 |
| Spastic Paraplegia 29, Autosomal Dominant |
|
Hyperactivity, Neonatal hyperbilirubinemia |
OMIM:609727 |
| Goodpasture Syndrome |
|
Glomerular crescent formation, Pallor, Glomerulonephritis, Erythrocyte cylindruria, Cylindruria, ... |
OMIM:233450 |
| X-Linked Creatine Transporter Deficiency |
|
Athetosis, Hyperactivity, Abnormal circulating creatine concentration, Ataxia |
ORPHA:52503 |
| Dextrocardia |
|
Abnormality of the ureter, Abnormal renal morphology |
ORPHA:1666 |
| Cone-Rod Dystrophy 8 |
|
Pallor |
OMIM:605549 |
| Tay-Sachs Disease |
|
Pallor |
OMIM:272800 |
| Renal-Hepatic-Pancreatic Dysplasia 1 |
|
Patent ductus arteriosus, Renal dysplasia, Stage 5 chronic kidney disease, Enlarged kidney, Polyc... |
OMIM:208540 |
| Blackfan-Diamond Anemia |
|
Hypospadias, Renal agenesis, Horseshoe kidney, Pallor |
ORPHA:124 |
| Oculocerebrorenal Syndrome Of Lowe |
|
Abnormal pupil morphology, Hyponatremia, Lentiglobus, Hypokalemia, Hypophosphatemia, Buphthalmos,... |
ORPHA:534 |
| Epidermolysis Bullosa Simplex With Pyloric Atresia |
|
Renal duplication, Aplasia of the bladder, Renal dysplasia, Glomerular sclerosis, Ureterocele, Ab... |
ORPHA:158684 |
| Diarrhea 10, Protein-Losing Enteropathy Type |
|
Polyuria, Death in infancy, Renal dysplasia |
OMIM:618183 |
| Intellectual Disability-Hypotonic Facies Syndrome, X-Linked, 1 |
|
Vesicoureteral reflux, Hyperactivity, Hypospadias, Renal hypoplasia, Micropenis |
OMIM:309580 |
| Cleft Lip/Palate-Ectodermal Dysplasia Syndrome |
|
Abnormality of the ureter |
ORPHA:3253 |
| Fibrous Dysplasia Of Bone |
|
Antalgic gait, Hypophosphatemia, Hypercalcemia, Difficulty walking |
ORPHA:249 |
| Bardet-Biedl Syndrome 12 |
|
Hydroureter, Cystic renal dysplasia, Hydronephrosis |
OMIM:615989 |
| Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 5 |
|
Hydroureter, Hydronephrosis, Megacystis |
OMIM:619431 |
| Charge Syndrome |
|
Patent ductus arteriosus, Arrhinencephaly, Renal agenesis, Horseshoe kidney, Dysphagia, Renal hyp... |
OMIM:214800 |
| Hyperparathyroidism-Jaw Tumor Syndrome |
|
Hypophosphatemia, Hypercalcemia, Polydipsia, Dysphagia |
ORPHA:99880 |
| Ellis Van Creveld Syndrome |
|
Renal hypoplasia/aplasia, Abnormality of the kidney, Hydroureter, Epispadias, Abnormality of the ... |
ORPHA:289 |
| Dent Disease 1 |
|
Hypophosphatemia |
OMIM:300009 |
| Vici Syndrome |
|
Abnormal posturing, Penile hypospadias, Dysphagia |
OMIM:242840 |
| Elliptocytosis 1 |
|
Pallor |
OMIM:611804 |
| Parathyroid Carcinoma |
|
Hypophosphatemia, Hypercalcemia, Polydipsia, Dysphagia |
ORPHA:143 |
| Metaphyseal Chondromatosis With D-2-Hydroxyglutaric Aciduria |
|
Dry skin, D-2-hydroxyglutaric aciduria, Unilateral renal agenesis |
ORPHA:99646 |
| Myopathy, Mitochondrial, And Ataxia |
|
Pallor |
OMIM:617675 |
| Short Rib-Polydactyly Syndrome, Verma-Naumoff Type |
|
Urethrovaginal fistula, Hypoplasia of penis, Renal cyst, Renal hypoplasia, Hydronephrosis |
ORPHA:93271 |
| Alternating Hemiplegia Of Childhood |
|
Dysphagia, Impulsivity, Oral-pharyngeal dysphagia, Pallor |
ORPHA:2131 |
| X-Linked Intellectual Disability-Acromegaly-Hyperactivity Syndrome |
|
Hyperactivity |
ORPHA:85327 |
| Orofaciodigital Syndrome Xiv |
|
Patent ductus arteriosus, Epispadias, Occipital encephalocele, Unilateral renal hypoplasia, Micro... |
OMIM:615948 |
| Letterer-Siwe Disease |
|
Pallor |
OMIM:246400 |
| Congenital Dyserythropoietic Anemia Type Iii |
|
Pallor |
ORPHA:98870 |
| Pyruvate Kinase Deficiency Of Red Cells |
|
Pallor |
OMIM:266200 |
| Ulbright-Hodes Syndrome |
|
Renal hypoplasia, Polycystic kidney dysplasia, Abnormal penis morphology |
ORPHA:3404 |
| Peters-Plus Syndrome |
|
Patent ductus arteriosus, Hypospadias, Renal hypoplasia, Ureteral duplication, Umbilical hernia, ... |
OMIM:261540 |
| Rare Circulatory System Disease |
|
Pallor |
ORPHA:98028 |
| Opsismodysplasia |
|
Hypophosphatemia |
OMIM:258480 |
| Primary Fanconi Renotubular Syndrome |
|
Hypophosphatemia, Hypokalemia, Decreased plasma carnitine, Hypophosphatemic rickets, Bicarbonatur... |
ORPHA:3337 |
| Hereditary Spherocytosis |
|
Skin ulcer, Pallor |
ORPHA:822 |
| Dominant Beta-Thalassemia |
|
Skin ulcer, Pallor |
ORPHA:231226 |
| Peutz-Jeghers Syndrome |
|
Abnormality of the ureter, Bladder polyp |
OMIM:175200 |
| Severe Combined Immunodeficiency Due To Complete Rag1/2 Deficiency |
|
Pallor |
ORPHA:331206 |
| Non-Functioning Pituitary Adenoma |
|
Pallor |
ORPHA:91349 |
| Acrorenal-Mandibular Syndrome |
|
Polycystic kidney dysplasia, Abnormality of the ureter, Renal agenesis, Aplasia of the bladder |
OMIM:200980 |
| Dent Disease |
|
Cataract, Renal hypophosphatemia, Elevated circulating creatine kinase concentration |
ORPHA:1652 |
| Thyrotoxic Periodic Paralysis |
|
Episodic hypokalemia, Transient hypophosphatemia, Hyperkalemia, Mildly elevated creatine kinase, ... |
ORPHA:79102 |
| Familial Hypocalciuric Hypercalcemia |
|
Hypocalcemic seizures, Renal hypophosphatemia, Hypercalcemia, Hypermagnesemia |
ORPHA:405 |
| Igg4-Related Kidney Disease |
|
Nephrotic range proteinuria, Hydronephrosis, Tubulointerstitial nephritis, Abnormal ureter morpho... |
ORPHA:449395 |
| Severe Congenital Hypochromic Anemia With Ringed Sideroblasts |
|
Pallor |
ORPHA:300298 |
| Aregenerative Anemia |
|
Pallor |
ORPHA:101096 |
| Mccune-Albright Syndrome |
|
Hypophosphatemia |
ORPHA:562 |
| Thoracoabdominal Syndrome |
|
Patent ductus arteriosus, Anencephaly, Hypospadias, Renal agenesis |
OMIM:313850 |
| Pituitary Apoplexy |
|
Pallor |
ORPHA:95613 |
| Raine Syndrome |
|
Hypophosphatemia |
OMIM:259775 |
| Beta-Thalassemia Major |
|
Skin ulcer, Pallor |
ORPHA:231214 |
| Systemic Mastocytosis With Associated Hematologic Neoplasm |
|
Pallor |
ORPHA:98849 |
| Schwartz-Jampel Syndrome |
|
Death in infancy, Abnormality of the ureter, Attention deficit hyperactivity disorder, Abnormalit... |
ORPHA:800 |
| Prolactinoma |
|
Pallor |
ORPHA:2965 |
| Sandifer Syndrome |
|
Abnormal posturing |
ORPHA:71272 |
| Argininemia |
|
Hyperactivity, Hyperammonemia, Hyperargininemia, Spastic gait |
OMIM:207800 |
| Oeis Complex |
|
Myelomeningocele, Vesicovaginal fistula, Hydroureter, Renal agenesis, Epispadias, Duplicated coll... |
OMIM:258040 |
| Retinitis Pigmentosa And Erythrocytic Microcytosis |
|
Pallor |
OMIM:616959 |
| Microphthalmia, Syndromic 6 |
|
Renal hypoplasia |
OMIM:607932 |
| Schinzel-Giedion Syndrome |
|
Nephroblastoma, Neural tube defect, Renal cyst, Abnormality of the ureter, Hypospadias, Dysphagia... |
ORPHA:798 |
| Meckel Syndrome, Type 1 |
|
Patent ductus arteriosus, Hypoplasia of the bladder, Polycystic kidney dysplasia, Cystic renal dy... |
OMIM:249000 |
| Incontinentia Pigmenti |
|
Erythema, Pallor |
OMIM:308300 |
| Refractory Anemia With Excess Blasts |
|
Anemic pallor |
ORPHA:86839 |
| Diphallia |
|
Renal duplication, Renal malrotation, Penoscrotal transposition, Epispadias, Hypospadias, Bifid p... |
ORPHA:227 |
| Fructose Intolerance, Hereditary |
|
Bicarbonaturia, Hypophosphatemia, Hyperuricemia, Hyperbilirubinemia |
OMIM:229600 |
| Idiopathic Hypereosinophilic Syndrome |
|
Dysphagia, Pallor |
ORPHA:3260 |
| Familial Gestational Hyperthyroidism |
|
Hyperactivity, Agitation |
ORPHA:99819 |
| Autosomal Recessive Hypophosphatemic Rickets |
|
Hypocalcemic tetany, Hypophosphatemic rickets, Renal hypophosphatemia |
ORPHA:289176 |
| Lipodystrophy, Familial Partial, Type 7 |
|
Dysphagia, Polyuria, Dry skin, Facial wrinkling |
OMIM:606721 |
| Microphthalmia, Syndromic 1 |
|
Renal hypoplasia, Hydroureter, Hypospadias, Renal hypoplasia/aplasia |
OMIM:309800 |
| Vater/Vacterl Association |
|
Patent ductus arteriosus, Vesicoureteral reflux, Renal dysplasia, Spina bifida, Renal agenesis, P... |
OMIM:192350 |
| Hypophosphatemic Rickets |
|
Hypophosphatemia, Hypercalcemia |
ORPHA:437 |
| Congenital Tracheal Stenosis |
|
Patent ductus arteriosus, Abnormality of the kidney, Abnormality of the ureter |
ORPHA:141127 |
| Autosomal Recessive Malignant Osteopetrosis |
|
Hypophosphatemia, Hypocalcemia |
ORPHA:667 |
| Microcephaly 29, Primary, Autosomal Recessive |
|
Hyperactivity, Ataxia |
OMIM:620047 |
| X-Linked Hypophosphatemia |
|
Hypophosphatemia |
ORPHA:89936 |
| Generalized Juvenile Polyposis/Juvenile Polyposis Coli |
|
Anemic pallor |
ORPHA:329971 |
| Tsh-Secreting Pituitary Adenoma |
|
Pallor |
ORPHA:91347 |
| Unilateral Polymicrogyria |
|
Pseudobulbar paralysis, Abnormal posturing |
ORPHA:268943 |
| Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 3 |
|
Pallor |
OMIM:253280 |
| Congenital Total Pulmonary Venous Return Anomaly |
|
Patent ductus arteriosus, Pallor |
ORPHA:99125 |
