Hemoglobin D Disease |
|
Anemia, Reduced alpha/beta synthesis ratio, HbS hemoglobin, Increased HbA2 hemoglobin, Reduced he... |
ORPHA:90039 |
Hereditary Persistence Of Fetal Hemoglobin-Beta-Thalassemia Syndrome |
|
Anemia, Persistence of hemoglobin F, Pallor, Hepatomegaly, Splenomegaly |
ORPHA:46532 |
Anemia, Congenital Dyserythropoietic, Type Ib |
|
Anemia, Jaundice, Erythroid hyperplasia, Reticulocytosis, Pallor, Poikilocytosis, Anisocytosis, H... |
OMIM:615631 |
Gjc2-Related Late-Onset Primary Lymphedema |
|
Pedal edema, Edema of the dorsum of hands, Predominantly lower limb lymphedema, Venous insufficie... |
ORPHA:568051 |
Autoimmune Hemolytic Anemia, Cold Type |
|
Hemolytic anemia, Abnormal leukocyte morphology, Splenomegaly, Pallor |
ORPHA:228312 |
Pyruvate Kinase Deficiency Of Red Cells |
|
Splenomegaly, Jaundice, Nonimmune hydrops fetalis, Reticulocytosis, Pallor, Erythroid hyperplasia... |
OMIM:266200 |
Hb Bart'S Hydrops Fetalis |
|
Polyhydramnios, Anemia, Hydrops fetalis, Pallor, Oligohydramnios, Hepatomegaly, Abnormal hemoglob... |
ORPHA:163596 |
X-Linked Sideroblastic Anemia |
|
Anemia, Elevated hepatic transaminase, Splenomegaly, Pallor |
ORPHA:75563 |
Acquired Idiopathic Sideroblastic Anemia |
|
Acute myeloid leukemia, Neutropenia, Megaloblastic erythroid hyperplasia, Granulocytopenia, Normo... |
ORPHA:75564 |
Lymphatic Malformation 9 |
|
Predominantly lower limb lymphedema, Tortuous lymphatic vessels |
OMIM:619319 |
Beta-Thalassemia |
|
Anemia, Hepatitis, Skin ulcer, Pallor, Hepatomegaly, Cholelithiasis, Thrombocytopenia, Abnormal h... |
ORPHA:848 |
Anemia, Hypochromic Microcytic, With Iron Overload 2 |
|
Anemia, Pallor, Poikilocytosis, Decreased mean corpuscular volume, Hepatomegaly, Elevated hepatic... |
OMIM:615234 |
Lymphatic Malformation 1 |
|
Predominantly lower limb lymphedema, Nonimmune hydrops fetalis, Prominent superficial veins, Hypo... |
OMIM:153100 |
Primary Intestinal Lymphangiectasia |
|
Peritoneal effusion, Anemia, Reduced proportion of CD4+ effector memory T cells, Pericardial effu... |
ORPHA:90362 |
Leishmaniasis |
|
Leukopenia, Anemia, Abnormal macrophage morphology, Skin ulcer, Elevated hepatic transaminase, Pa... |
ORPHA:507 |
Primary Myelofibrosis |
|
Anemia, Petechiae, Extramedullary hematopoiesis, Purpura, Pancytopenia, Hepatosplenomegaly, Pallo... |
ORPHA:824 |
Lymphatic Malformation 5 |
|
Predominantly lower limb lymphedema, Hypoplasia of lymphatic vessels, Facial edema |
OMIM:153200 |
Congenital Disorder Of Glycosylation, Type Ib |
|
Lymphangiectasis, Hepatic failure, Hepatic fibrosis, Cirrhosis, Edema, Hepatomegaly |
OMIM:602579 |
Yellow Nail Syndrome |
|
Predominantly lower limb lymphedema, Hypoplasia of lymphatic vessels, Lymphedema |
OMIM:153300 |
Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema |
|
Exercise-induced hemolysis, Increased mean corpuscular hemoglobin concentration, Splenomegaly, He... |
OMIM:194380 |
Kaposiform Lymphangiomatosis |
|
Pancreatic cysts, Anemia, Epidural hemorrhage, Pericardial effusion, Abnormal spleen morphology, ... |
ORPHA:464329 |
Elliptocytosis 1 |
|
Hemolytic anemia, Elliptocytosis, Jaundice, Pallor, Splenomegaly |
OMIM:611804 |
Lymphangioleiomyomatosis |
|
Pulmonary lymphangiomyomatosis |
OMIM:606690 |
Cold Agglutinin Disease |
|
Hemolytic anemia, Pallor, Lymphadenopathy, Hepatomegaly, Splenomegaly |
ORPHA:56425 |
Beta-Thalassemia Intermedia |
|
Cirrhosis, Splenomegaly, Abnormality of the liver, Increased HbA2 hemoglobin, Jaundice, Skin ulce... |
ORPHA:231222 |
Anemia, Nonspherocytic Hemolytic, Due To G6Pd Deficiency |
|
Heinz bodies, Jaundice, Fava bean-induced hemolytic anemia, Reticulocytosis, Pallor, Poikilocytos... |
OMIM:300908 |
Deafness-Lymphedema-Leukemia Syndrome |
|
Lymphedema, Intracranial hemorrhage, Pallor, Lymphadenopathy, Abnormal neutrophil count, Hepatome... |
ORPHA:3226 |
Kasabach-Merritt Syndrome |
|
Leukopenia, Anemia, Petechiae, Microangiopathic hemolytic anemia, Purpura, Reticulocytosis, Hepat... |
ORPHA:2330 |
Acute Myelomonocytic Leukemia |
|
Anemia, Pallor, Leukocytosis, Eosinophilia, Thrombocytopenia |
ORPHA:517 |
Myopathy, Lactic Acidosis, And Sideroblastic Anemia 2 |
|
Sideroblastic anemia, Elevated hepatic transaminase, Hepatomegaly, Pallor |
OMIM:613561 |
Acute Peripheral Arterial Occlusion |
|
Stroke, Leukocytosis, Pallor |
ORPHA:90064 |
Beta-Thalassemia, Dominant Inclusion Body Type |
|
Increased HbA2 hemoglobin, Decreased mean corpuscular hemoglobin concentration, Persistence of he... |
OMIM:603902 |
Hereditary Spherocytosis |
|
Increased mean corpuscular hemoglobin concentration, Anemia, Spontaneous hemolytic crises, Jaundi... |
ORPHA:822 |
Hennekam Lymphangiectasia-Lymphedema Syndrome 2 |
|
Pulmonary lymphangiectasia, Intestinal lymphangiectasia, Pericardial lymphangiectasia, Lymphedema |
OMIM:616006 |
Severe Congenital Hypochromic Anemia With Ringed Sideroblasts |
|
Anemia, Reticulocytopenia, Dysplastic erythropoesis, Anisopoikilocytosis, Elevated hepatic transa... |
ORPHA:300298 |
Megaloblastic Anemia Due To Dihydrofolate Reductase Deficiency |
|
Megaloblastic anemia, Jaundice, Pancytopenia, Pallor, Hepatomegaly, Increased circulating lactate... |
OMIM:613839 |
Yellow Nail Syndrome |
|
Lymphedema, Hypoplasia of lymphatic vessels, Biliary tract neoplasm |
ORPHA:662 |
Parkes Weber Syndrome |
|
Vascular dilatation, Arteriovenous malformation, Cerebral arteriovenous malformation, Skin ulcer,... |
ORPHA:90307 |
Breath-Holding Spells |
|
Iron deficiency anemia, Pallor |
OMIM:607578 |
Congenital Dyserythropoietic Anemia Type Iii |
|
Anemia, Elevated hepatic transaminase, Poikilocytosis, Abnormal erythrocyte morphology, Pallor, A... |
ORPHA:98870 |
Renal Tubular Acidosis, Distal, 4, With Hemolytic Anemia |
|
Hemolytic anemia, Reticulocytosis, Pallor, Decreased mean corpuscular volume, Hepatosplenomegaly |
OMIM:611590 |
Hemolytic Anemia Due To Red Cell Pyruvate Kinase Deficiency |
|
Anemia, Hydrops fetalis, Congenital hemolytic anemia, Reticulocytosis, Poikilocytosis, Abnormal e... |
ORPHA:766 |
Lymphangiectasia, Intestinal |
|
Pedal edema, Lymphopenia, Edema, Stillbirth, Intestinal lymphangiectasia |
OMIM:152800 |
Retinitis Pigmentosa 27 |
|
Macular edema, Pallor |
OMIM:613750 |
Evans Syndrome |
|
Petechiae, Neutropenia in presence of anti-neutropil antibodies, Jaundice, Pallor, Autoimmune thr... |
ORPHA:1959 |
American Trypanosomiasis |
|
Pallor, Edema, Lymphadenopathy, Hepatomegaly, Periorbital edema, Splenomegaly |
ORPHA:3386 |
Anemia, Sideroblastic, 1 |
|
Sideroblastic anemia, Hypochromic microcytic anemia, Macrocytic anemia, Anemic pallor, Anemia of ... |
OMIM:300751 |
Alpha-Thalassemia |
|
Anemia, Hydrops fetalis, Hemolytic anemia, Hypersplenism, Jaundice, Cholelithiasis, Abnormal hemo... |
ORPHA:846 |
Methylmalonic Acidemia With Homocystinuria, Type Cbld |
|
Pallor |
ORPHA:79283 |
Dominant Beta-Thalassemia |
|
Hepatic fibrosis, Cirrhosis, Hypersplenism, Jaundice, Skin ulcer, Hepatocellular carcinoma, Reduc... |
ORPHA:231226 |
Severe Combined Immunodeficiency Due To Complete Rag1/2 Deficiency |
|
Lymphadenitis, Abnormal natural killer cell count, Decreased proportion of CD3-positive T cells, ... |
ORPHA:331206 |
Beta-Thalassemia Major |
|
Hepatic fibrosis, Cirrhosis, Hypersplenism, Jaundice, Skin ulcer, Hepatocellular carcinoma, Aniso... |
ORPHA:231214 |
Peripheral Cone Dystrophy |
|
Pallor |
OMIM:609021 |
Letterer-Siwe Disease |
|
Anemia, Jaundice, Pallor, Hepatosplenomegaly, Thrombocytopenia, Neutropenia |
OMIM:246400 |
Cone-Rod Dystrophy 11 |
|
Pallor |
OMIM:610381 |
Autoimmune Hemolytic Anemia |
|
Hemolytic anemia, Abnormal leukocyte morphology, Splenomegaly, Pallor |
ORPHA:98375 |
Chromomycosis |
|
Lymphangiectasis, Predominantly lower limb lymphedema, Edema, Lymphedema |
ORPHA:182 |
Thiamine-Responsive Megaloblastic Anemia Syndrome |
|
Stroke, Thrombocytopenia, Megaloblastic anemia, Pallor |
ORPHA:49827 |
Autoimmune Hemolytic Anemia, Warm Type |
|
Chronic lymphatic leukemia, Jaundice, Pallor, Autoimmune hemolytic anemia, Splenomegaly |
ORPHA:90033 |
Myelofibrosis |
|
Myeloproliferative disorder, Purpura, Splenomegaly, Pallor |
OMIM:254450 |
Mullerian Derivatives, Persistence Of, With Lymphangiectasia And Postaxial Polydactyly |
|
Polyhydramnios, Hepatic failure, Lymphedema, Thyroid lymphangiectasia, Pulmonary lymphangiectasia... |
OMIM:235255 |
Systemic Mastocytosis With Associated Hematologic Neoplasm |
|
Acute myeloid leukemia, Myeloid leukemia, Increased basophil count, Chronic lymphatic leukemia, E... |
ORPHA:98849 |
Waldenström Macroglobulinemia |
|
Pedal edema, Leukemia, Normocytic anemia, Purpura, Pallor, Pleural effusion, Abnormality of neutr... |
ORPHA:33226 |
Pearson Marrow-Pancreas Syndrome |
|
Hepatic failure, Hydrops fetalis, Anemia, Reticulocytopenia, Exocrine pancreatic insufficiency, R... |
OMIM:557000 |
Drug-Induced Autoimmune Hemolytic Anemia |
|
Autoimmune hemolytic anemia, Splenomegaly, Pallor |
ORPHA:90037 |
Optic Atrophy 1 |
|
Pallor |
OMIM:165500 |
Dermatitis, Atopic |
|
Facial erythema, Dry skin, Pallor |
OMIM:603165 |
Anemia, Congenital Dyserythropoietic, Type Ia |
|
Hydrops fetalis, Hemolytic anemia, Erythroid hyperplasia, Reticulocytosis, Reduced level of N-ace... |
OMIM:224120 |
Benign Paroxysmal Torticollis Of Infancy |
|
Pallor |
ORPHA:71518 |
Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency |
|
Diffuse pancreatic islet hyperplasia, Focal pancreatic islet hyperplasia, Hepatomegaly, Pallor |
ORPHA:276575 |
Sepsis In Premature Infants |
|
Anemia, Petechiae, Jaundice, Purpura, Pallor, Edema, Hepatomegaly, Leukocytosis, Decreased liver ... |
ORPHA:90051 |
Osteoporosis-Oculocutaneous Hypopigmentation Syndrome |
|
Pallor |
ORPHA:2786 |
Hyperinsulinism Due To Ucp2 Deficiency |
|
Diffuse pancreatic islet hyperplasia, Hepatomegaly, Pallor |
ORPHA:276556 |
Aregenerative Anemia |
|
Reticulocytopenia, Abnormal proportion of CD8-positive T cells, Erythroid hypoplasia, Pallor, Pan... |
ORPHA:101096 |
Imerslund-Gräsbeck Syndrome |
|
Megaloblastic anemia, Anisopoikilocytosis, Abnormal hemoglobin concentration, Reticulocytosis, Pa... |
ORPHA:35858 |
Idiopathic Pulmonary Hemosiderosis |
|
Iron deficiency anemia, Pallor, Hepatomegaly, Hepatosplenomegaly |
ORPHA:99931 |
Leber Congenital Amaurosis 14 |
|
Pallor |
OMIM:613341 |
Autosomal Dominant Hyperinsulinism Due To Kir6.2 Deficiency |
|
Diffuse pancreatic islet hyperplasia, Hepatomegaly, Pallor |
ORPHA:276580 |
Senior-Loken Syndrome 8 |
|
Pancreatic cysts, Vascular dilatation, Intrahepatic bile duct dilatation, Pallor, Hepatic cysts |
OMIM:616307 |
Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome |
|
Pancreatic islet-cell hyperplasia, Pallor |
ORPHA:276608 |
Irida Syndrome |
|
Pallor, Intrahepatic cholestasis |
ORPHA:209981 |
Complement Hyperactivation, Angiopathic Thrombosis, And Protein-Losing Enteropathy |
|
Anemia, Edema, Thrombocytosis, Hepatomegaly, Iron deficiency anemia, Ascites, Intestinal lymphang... |
OMIM:226300 |
Hennekam Lymphangiectasia-Lymphedema Syndrome 1 |
|
Lymphedema, Thyroid lymphangiectasia, Pericardial effusion, Pulmonary lymphangiectasia, Nonimmune... |
OMIM:235510 |
Lymphatic Filariasis |
|
Lymphadenitis, Lymphangiectasis, Hypereosinophilia, Lymphedema, Predominantly lower limb lymphede... |
ORPHA:2035 |
Myopathy, Lactic Acidosis, And Sideroblastic Anemia 1 |
|
Pappenheimer bodies, Sideroblastic anemia, Erythroid hyperplasia, Pallor, Hypochromic anemia, Mic... |
OMIM:600462 |
Hyperinsulinism Due To Hnf1A Deficiency |
|
Hepatomegaly, Pallor |
ORPHA:324575 |
Overhydrated Hereditary Stomatocytosis |
|
Intermittent jaundice, Stomatocytosis, Hemolytic anemia, Abnormal mean corpuscular volume, Decrea... |
ORPHA:3203 |
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency |
|
Anemia, Hepatomegaly, Pallor |
OMIM:246450 |
Idiopathic Hypereosinophilic Syndrome |
|
Elevated hepatic transaminase, Generalized lymphadenopathy, Hepatosplenomegaly, Pleural effusion,... |
ORPHA:3260 |
Primary Lateral Sclerosis, Juvenile |
|
Pallor |
OMIM:606353 |
Optic Atrophy 7 With Or Without Auditory Neuropathy |
|
Pallor |
OMIM:612989 |
Retinitis Pigmentosa And Erythrocytic Microcytosis |
|
Anemia, Elliptocytosis, Poikilocytosis, Pallor, Anisocytosis, Decreased mean corpuscular volume |
OMIM:616959 |
Lymphangiectasia, Pulmonary, Congenital |
|
Polyhydramnios, Pedal edema, Pulmonary lymphangiectasia, Nonimmune hydrops fetalis, Pleural effus... |
OMIM:265300 |
3-Hydroxy-3-Methylglutaric Aciduria |
|
Leukopenia, Anemia, Jaundice, Elevated hepatic transaminase, Pallor, Edema, Acute pancreatitis, T... |
ORPHA:20 |
Familial Focal Epilepsy With Variable Foci |
|
Pallor |
ORPHA:98820 |
Hyperinsulinism Due To Hnf4A Deficiency |
|
Elevated hepatic transaminase, Pallor, Increased hepatic glycogen content, Elevated circulating a... |
ORPHA:263455 |
Aplasia Cutis Congenita With Intestinal Lymphangiectasia |
|
Lymphopenia, Intestinal lymphangiectasia, Generalized edema |
OMIM:207731 |
Hereditary Elliptocytosis |
|
Stomatocytosis, Hydrops fetalis, Congenital hemolytic anemia, Hemolytic anemia, Elliptocytosis, J... |
ORPHA:288 |
Lymphatic Malformation 6 |
|
Polyhydramnios, Splenomegaly, Webbed neck, Lymphedema, Nonimmune hydrops fetalis, Pleural effusio... |
OMIM:616843 |
Refractory Anemia With Excess Blasts |
|
Pedal edema, Acute myeloid leukemia, Abnormal mean corpuscular volume, Leukocytosis, Anemic pallo... |
ORPHA:86839 |
Müllerian Derivatives-Lymphangiectasia-Polydactyly Syndrome |
|
Polyhydramnios, Hepatic failure, Pulmonary lymphangiectasia, Redundant neck skin, Hepatosplenomeg... |
ORPHA:1655 |
Fumarase Deficiency |
|
Hepatic failure, Polycythemia, Cholestasis, Pallor |
OMIM:606812 |
Beta-Ketothiolase Deficiency |
|
Pallor, Edema, Thrombocytosis, Leukocytosis, Dehydration, Hepatomegaly |
ORPHA:134 |
Spontaneous Periodic Hypothermia |
|
Pallor |
ORPHA:29822 |
Blackfan-Diamond Anemia |
|
Acute myeloid leukemia, Leukopenia, Webbed neck, Reticulocytopenia, Radial artery aplasia, Pure r... |
ORPHA:124 |
Fructose-1,6-Bisphosphatase Deficiency |
|
Elevated hepatic transaminase, Abnormal circulating enzyme concentration or activity, Pallor, Hep... |
ORPHA:348 |
Cyclic Vomiting Syndrome |
|
Pallor |
OMIM:500007 |
Rare Circulatory System Disease |
|
Arterial calcification, Pallor, Abnormal systemic arterial morphology, Arterial tortuosity, Vascu... |
ORPHA:98028 |
Kcnq2-Related Epileptic Encephalopathy |
|
Facial erythema, Cerebral edema, Pallor |
ORPHA:439218 |
Retinitis Pigmentosa 51 |
|
Pallor |
OMIM:613464 |
Hereditary Folate Malabsorption |
|
Megaloblastic anemia, Pancytopenia, Pallor, Eosinophilia, Thrombocytopenia |
ORPHA:90045 |
Mixed-Type Autoimmune Hemolytic Anemia |
|
Autoimmune hemolytic anemia, Pallor |
ORPHA:90036 |
Non-Functioning Paraganglioma |
|
Cerebral hemorrhage, Pallor |
ORPHA:94080 |
Myopathic Ehlers-Danlos Syndrome |
|
Pallor |
ORPHA:536516 |
Plummer-Vinson Syndrome |
|
Hypochromic microcytic anemia, Iron deficiency anemia, Pallor |
ORPHA:54028 |
Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome |
|
Lymphedema, Dermal translucency, Pulmonary lymphangiectasia, Nonimmune hydrops fetalis, Palpebral... |
OMIM:137940 |
Dravet Syndrome |
|
Pallor |
ORPHA:33069 |
Lymphedema-Hypoparathyroidism Syndrome |
|
Pulmonary lymphangiectasia, Lymphedema |
OMIM:247410 |
Costello Syndrome |
|
Polyhydramnios, Lymphangiectasis, Webbed neck, Redundant neck skin |
OMIM:218040 |
Generalized Juvenile Polyposis/Juvenile Polyposis Coli |
|
Anemic pallor, Edema, Anemia |
ORPHA:329971 |
Cone-Rod Dystrophy 8 |
|
Retinal arteriolar constriction, Pallor |
OMIM:605549 |
Tay-Sachs Disease |
|
Cherry red spot of the macula, Pallor |
OMIM:272800 |
Diamond-Blackfan Anemia 1 |
|
Webbed neck, Reticulocytopenia, Pallor, Coarctation of aorta, Thrombocytosis, Thrombocytopenia, N... |
OMIM:105650 |
Fanconi Anemia, Complementation Group I |
|
Neutropenia, Pallor |
OMIM:609053 |
Autosomal Recessive Malignant Osteopetrosis |
|
Anemia, Pallor, Lymphadenopathy, Pulmonary artery stenosis, Hepatomegaly, Splenomegaly |
ORPHA:667 |
Hennekam Syndrome |
|
Hydrops fetalis, Lymphedema, Arteriovenous malformation, Pericardial effusion, Pulmonary lymphang... |
ORPHA:2136 |
Rheumatic Fever |
|
Erythema, Pallor |
ORPHA:3099 |
6-Pyruvoyl-Tetrahydropterin Synthase Deficiency |
|
Pallor |
ORPHA:13 |
Retinitis Pigmentosa 75 |
|
Pallor |
OMIM:617023 |
Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins |
|
Patent ductus arteriosus, Asplenia, Polyhydramnios, Interrupted aortic arch, Pulmonary lymphangie... |
OMIM:265380 |
Fanconi Anemia, Complementation Group E |
|
Anemia, Reticulocytopenia, Pancytopenia, Anemic pallor, Thrombocytopenia, Neutropenia, Leukemia |
OMIM:600901 |
Von Hippel-Lindau Disease |
|
Pancreatic cysts, Macular edema, Neoplasm of the pancreas, Polycythemia, Pallor, Pancreatic islet... |
ORPHA:892 |
Fanconi Anemia, Complementation Group D2 |
|
Patent ductus arteriosus, Anemia, Reticulocytopenia, Pancytopenia, Annular pancreas, Anemic pallo... |
OMIM:227646 |
Infection-Related Hemolytic Uremic Syndrome |
|
Pleural empyema, Hemolytic anemia, Pallor, Edema, Leukocytosis, Thrombocytopenia, Pancreatitis, G... |
ORPHA:544482 |
Fanconi Anemia, Complementation Group A |
|
Anemia, Reticulocytopenia, Pancytopenia, Anemic pallor, Thrombocytopenia, Neutropenia, Leukemia |
OMIM:227650 |
Histiocytoid Cardiomyopathy |
|
Stroke-like episode, Pulmonary edema, Hepatomegaly, Pallor |
ORPHA:137675 |
Degcags Syndrome |
|
Patent ductus arteriosus, Polyhydramnios, Anemia, Leukopenia, Abnormal spleen morphology, Pancyto... |
OMIM:619488 |
Sporadic Pheochromocytoma/Secreting Paraganglioma |
|
Cerebral hemorrhage, Pallor |
ORPHA:276621 |
Adenohypophysitis |
|
Normochromic anemia, Pallor |
ORPHA:95512 |
Non-Functioning Pituitary Adenoma |
|
Anemia of inadequate production, Pallor |
ORPHA:91349 |
Panhypophysitis |
|
Normochromic anemia, Pallor |
ORPHA:95513 |
Pituitary Apoplexy |
|
Normochromic anemia, Pallor |
ORPHA:95613 |
Fanconi Anemia, Complementation Group C |
|
Anemia, Reticulocytopenia, Pancytopenia, Anemic pallor, Thrombocytopenia, Neutropenia, Leukemia |
OMIM:227645 |
Myopathy, Mitochondrial, And Ataxia |
|
Pallor |
OMIM:617675 |
Sheehan Syndrome |
|
Dry skin, Normochromic anemia, Pallor |
ORPHA:91355 |
Childhood Absence Epilepsy |
|
Pallor |
ORPHA:64280 |
Multiple Endocrine Neoplasia Type 2 |
|
Pallor, Neoplasm of the liver, Cervical lymphadenopathy |
ORPHA:653 |
Hereditary Pheochromocytoma-Paraganglioma |
|
Cerebral hemorrhage, Pallor |
ORPHA:29072 |
Incontinentia Pigmenti |
|
Leukocytosis, Eosinophilia, Erythema, Pallor |
OMIM:308300 |
Esophageal Atresia |
|
Pallor, Tetralogy of Fallot, Polyhydramnios, Coarctation of aorta |
ORPHA:1199 |
Alternating Hemiplegia Of Childhood |
|
Dehydration, Pallor |
ORPHA:2131 |
Prolactinoma |
|
Pallor |
ORPHA:2965 |
Congenital Total Pulmonary Venous Return Anomaly |
|
Patent ductus arteriosus, Double outlet right ventricle, Cardiac total anomalous pulmonary venous... |
ORPHA:99125 |
Tsh-Secreting Pituitary Adenoma |
|
Pericardial effusion, Pallor |
ORPHA:91347 |
Lymphangioleiomyomatosis |
|
Lymphedema, Chylopericardium, Lymphadenopathy, Chylothorax, Ascites, Abnormality of the lymphatic... |
ORPHA:538 |
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 3 |
|
Pallor |
OMIM:253280 |
Goodpasture Syndrome |
|
Anemia, Pallor |
OMIM:233450 |
Tuberous Sclerosis Complex |
|
Hepatic cysts, Aortic aneurysm, Pulmonary lymphangiomyomatosis |
ORPHA:805 |
Tuberous Sclerosis 1 |
|
Pulmonary lymphangiomyomatosis |
OMIM:191100 |
Tuberous Sclerosis 2 |
|
Pulmonary lymphangiomyomatosis |
OMIM:613254 |
Hennekam Lymphangiectasia-Lymphedema Syndrome 3 |
|
Polyhydramnios, Lymphedema |
OMIM:618154 |