| Thrombocytopenia 4 |
|
Thrombocytopenia, Abnormal platelet volume |
OMIM:612004 |
| Bleeding Disorder, Platelet-Type, 15 |
|
Platelet anisocytosis, Thrombocytopenia, Increased mean platelet volume |
OMIM:615193 |
| Thrombocytopenia 3 |
|
Thrombocytopenia, Decreased mean platelet volume |
OMIM:273900 |
| Bleeding Disorder, Platelet-Type, 16 |
|
Anemia, Impaired platelet aggregation, Thrombocytopenia, Giant platelets, Platelet anisocytosis, ... |
OMIM:187800 |
| Storage Pool Platelet Disease |
|
Decreased mean platelet volume, Acute leukemia |
OMIM:185050 |
| Macrothrombocytopenia, Isolated, 2, Autosomal Dominant |
|
Macrothrombocytopenia |
OMIM:619840 |
| Bleeding Disorder, Platelet-Type, 24 |
|
Impaired arachidonic acid-induced platelet aggregation, Impaired ADP-induced platelet aggregation... |
OMIM:619271 |
| Platelet Glycoprotein Iv Deficiency |
|
Thrombocytopenia, Giant platelets |
OMIM:608404 |
| Thrombocytopenia 1 |
|
Congenital thrombocytopenia, Decreased mean platelet volume, Intermittent thrombocytopenia, Joint... |
OMIM:313900 |
| Combined Oxidative Phosphorylation Deficiency 38 |
|
Decreased activity of mitochondrial ATP synthase complex, Delayed speech and language development... |
OMIM:618378 |
| Thrombocytopenia With Beta-Thalassemia, X-Linked |
|
Splenomegaly, Hemolytic anemia, Reticulocytosis, Increased RBC distribution width, Thrombocytopen... |
OMIM:314050 |
| Barth Syndrome |
|
Abnormal mitochondrial morphology |
ORPHA:111 |
| Giant platelet syndrome with thrombocytopenia |
|
Thrombocytopenia, Giant platelets |
OMIM:137560 |
| Metaphyseal Modeling Abnormality, Skin Lesions, And Spastic Paraplegia |
|
Increased bone mineral density |
OMIM:250500 |
| Paragangliomas 6 |
|
Elevated circulating catecholamine level, Paraganglioma |
OMIM:618464 |
| Leber Congenital Amaurosis 10 |
|
Hyposmia |
OMIM:611755 |
| Osteoporosis |
|
Osteoporosis |
OMIM:166710 |
| Pyknoachondrogenesis |
|
Increased bone mineral density |
OMIM:265880 |
| Macrothrombocytopenia And Granulocyte Inclusions With Or Without Nephritis Or Sensorineural Hearing Loss |
|
Impaired ADP-induced platelet aggregation, Impaired epinephrine-induced platelet aggregation, Leu... |
OMIM:155100 |
| Melorheostosis, Isolated |
|
Increased bone mineral density, Hyperostosis |
OMIM:155950 |
| Hypogonadotropic Hypogonadism 17 With Or Without Anosmia |
|
Hyposmia |
OMIM:615266 |
| Macrothrombocytopenia, Isolated, 1, Autosomal Dominant |
|
Macrothrombocytopenia, Impaired platelet aggregation |
OMIM:613112 |
| Bleeding Disorder, Platelet-Type, 21 |
|
Thrombocytopenia, Impaired ADP-induced platelet aggregation, Increased mean platelet volume, Impa... |
OMIM:617443 |
| Hypogonadotropic Hypogonadism 21 With Or Without Anosmia |
|
Hyposmia |
OMIM:615271 |
| Bernard-Soulier Syndrome |
|
Thrombocytopenia, Macrothrombocytopenia, Impaired ristocetin-induced platelet aggregation, Giant ... |
OMIM:231200 |
| Dna2-Related Mitochondrial Dna Deletion Syndrome |
|
Decreased mitochondrial number, Gait disturbance, Difficulty walking |
ORPHA:352470 |
| Hsd10 Mitochondrial Disease |
|
Delayed speech and language development, Choreoathetosis, Abnormal mitochondrial morphology |
OMIM:300438 |
| Charcot-Marie-Tooth Disease, Axonal, Mitochondrial Form, 1 |
|
Neurogenic bladder, Decreased activity of mitochondrial complex III, Decreased activity of mitoch... |
OMIM:500013 |
| Huntington Disease |
|
Gait imbalance, Inability to walk, Gait disturbance, Difficulty walking, Speech articulation diff... |
ORPHA:399 |
| Myh9-Related Disease |
|
Congenital thrombocytopenia, Neutrophil inclusion bodies, Increased mean platelet volume, Giant p... |
ORPHA:182050 |
| Autosomal Dominant Mitochondrial Myopathy With Exercise Intolerance |
|
Increased mitochondrial number |
ORPHA:457050 |
| Immunodeficiency 71 With Inflammatory Disease And Congenital Thrombocytopenia |
|
Lymphocytosis, Thrombocytopenia, Decreased mean platelet volume |
OMIM:617718 |
| Slc35A1-Cdg |
|
Thrombocytopenia, Neutropenia, Abnormal platelet granules, Giant platelets |
ORPHA:238459 |
| Hypogonadotropic Hypogonadism 7 With Or Without Anosmia |
|
Abnormality of the sense of smell |
OMIM:146110 |
| Wiskott-Aldrich Syndrome |
|
Absent microvilli on the surface of peripheral blood lymphocytes, Decreased proportion of CD8-pos... |
OMIM:301000 |
| Ghosal Hematodiaphyseal Dysplasia |
|
Leukopenia, Hyperostosis cranialis interna, Increased bone mineral density, Myelofibrosis, Refrac... |
OMIM:231095 |
| Peroxisome Biogenesis Disorder 9B |
|
Anosmia, Ataxia |
OMIM:614879 |
| Arrhinia-Choanal Atresia-Microphthalmia Syndrome |
|
Aplasia/Hypoplasia involving the nose, Abnormality of the sense of smell, Choanal atresia |
ORPHA:1135 |
| Deafness, Autosomal Dominant 1, With Or Without Thrombocytopenia |
|
Macrothrombocytopenia, Thrombocytopenia, Impaired platelet aggregation |
OMIM:124900 |
| Bernard-Soulier Syndrome, Type A2, Autosomal Dominant |
|
Stomatocytosis, Splenomegaly, Impaired collagen-related peptide-induced platelet aggregation, Hem... |
OMIM:153670 |
| Gnathodiaphyseal Dysplasia |
|
Increased susceptibility to fractures, Osteomyelitis, Osteopenia, Diaphyseal cortical sclerosis |
OMIM:166260 |
| Mitochondrial Complex Iv Deficiency, Nuclear Type 19 |
|
Decreased activity of mitochondrial complex IV, Increased mitochondrial number |
OMIM:619063 |
| Anosmia For Butyl Mercaptan |
|
Anosmia |
OMIM:270350 |
| Isovaleric Acid, Inability To Smell |
|
Anosmia |
OMIM:243450 |
| Anosmia, Isolated Congenital, X-Linked |
|
Anosmia |
OMIM:301700 |
| Anosmia, Isolated Congenital |
|
Anosmia |
OMIM:107200 |
| Anosmia For Isobutyric Acid |
|
Partial anosmia |
OMIM:207000 |
| Hypogonadotropic Hypogonadism 9 With Or Without Anosmia |
|
Anosmia, Bifid nose, Hyposmia |
OMIM:614838 |
| Thumb Agenesis, Short Stature, And Immunodeficiency |
|
Anosmia |
OMIM:274190 |
| Musk, Inability To Smell |
|
Anosmia |
OMIM:254150 |
| Mitochondrial Dna Depletion Syndrome 16 (Hepatic Type) |
|
Abnormal mitochondrial morphology |
OMIM:618528 |
| Leukoencephalopathy With Dystonia And Motor Neuropathy |
|
Azoospermia, Hyposmia |
OMIM:613724 |
| Bleeding Disorder, Platelet-Type, 19 |
|
Anemia, Thrombocytopenia, Macrothrombocytopenia |
OMIM:616176 |
| Combined Oxidative Phosphorylation Deficiency 18 |
|
Delayed speech and language development, Dysmetria, Decreased activity of mitochondrial complex I... |
OMIM:615578 |
| Spastic Paraplegia Type 7 |
|
Spastic gait, Abnormal mitochondrial morphology |
ORPHA:99013 |
| Chondrodysplasia Punctata 1, X-Linked Recessive |
|
Depressed nasal bridge, Short nasal septum, Anosmia, Short nose |
OMIM:302950 |
| Hypophosphatemic Rickets, Autosomal Recessive, 1 |
|
Rickets, Increased bone mineral density, Hypophosphatemic rickets, Craniosynostosis |
OMIM:241520 |
| Aural Atresia, Congenital |
|
Hyposmia |
OMIM:607842 |
| Dacryocystitis-Osteopoikilosis Syndrome |
|
Increased bone mineral density, Osteopoikilosis |
ORPHA:1562 |
| Apnea, Obstructive Sleep |
|
Anosmia |
OMIM:107650 |
| Thrombocytopenia With Congenital Dyserythropoietic Anemia |
|
Poikilocytosis, Anisocytosis, Hypochromic anemia, Macrothrombocytopenia, Anemia of inadequate pro... |
ORPHA:67044 |
| Hypogonadotropic Hypogonadism 2 With Or Without Anosmia |
|
Agenesis of corpus callosum, Anosmia, Hyposmia, Choanal atresia |
OMIM:147950 |
| Bardet-Biedl Syndrome 19 |
|
Hyposmia |
OMIM:615996 |
| Dnm1L-Related Encephalopathy Due To Mitochondrial And Peroxisomal Fission Defect |
|
Difficulty walking, Inability to walk, Abnormality of the mitochondrion, Absent speech |
ORPHA:330050 |
| Hypogonadotropic Hypogonadism 20 With Or Without Anosmia |
|
Anosmia |
OMIM:615270 |
| Sitosterolemia 1 |
|
Stomatocytosis, Anemia, Arthritis, Reticulocytosis, Impaired platelet aggregation, Episodic hemol... |
OMIM:210250 |
| Body Mass Index Quantitative Trait Locus 19 |
|
Anosmia, Hyposmia |
OMIM:617885 |
| Hypogonadotropic Hypogonadism 6 With Or Without Anosmia |
|
Anosmia, Hyposmia |
OMIM:612702 |
| Hypogonadotropic Hypogonadism 4 With Or Without Anosmia |
|
Anosmia, Hyposmia |
OMIM:610628 |
| Hypogonadotropic Hypogonadism 14 With Or Without Anosmia |
|
Anosmia |
OMIM:614858 |
| Frontotemporal Dementia With Motor Neuron Disease |
|
Progressive cerebellar ataxia, Abnormal mitochondrial morphology |
ORPHA:275872 |
| Hypogonadotropic Hypogonadism 5 With Or Without Anosmia |
|
Anosmia |
OMIM:612370 |
| Hypogonadotropic Hypogonadism 18 With Or Without Anosmia |
|
Anosmia |
OMIM:615267 |
| Kufor-Rakeb Syndrome |
|
Akinesia, Hyposmia, Gait disturbance, Ataxia, Anosmia |
OMIM:606693 |
| Hypogonadotropic Hypogonadism 3 With Or Without Anosmia |
|
Anosmia, Hyposmia |
OMIM:244200 |
| Pelger-Huet Anomaly |
|
Hyposegmentation of neutrophil nuclei, Abnormality of neutrophils, Giant platelets, Thrombocytope... |
OMIM:169400 |
| Intestinal Pseudoobstruction, Neuronal, Chronic Idiopathic, X-Linked |
|
Thrombocytopenia, Increased mean platelet volume |
OMIM:300048 |
| Oxoglutaric Aciduria |
|
Abnormality of Krebs cycle metabolism, Ataxia |
ORPHA:31 |
| Hypogonadotropic Hypogonadism 16 With Or Without Anosmia |
|
Anosmia, Azoospermia, Hyposmia |
OMIM:614897 |
| Hyperostosis Cranialis Interna |
|
Anosmia, Hyposmia |
OMIM:144755 |
| Hypogonadotropic Hypogonadism 1 With Or Without Anosmia |
|
Anosmia, Ataxia, Azoospermia, Hyposmia |
OMIM:308700 |
| Gorlin Syndrome |
|
Abnormality of the sense of smell, Wide nasal bridge |
ORPHA:377 |
| Neuropathy, Hereditary Motor And Sensory, Type Via, With Optic Atrophy |
|
Anosmia, Steppage gait |
OMIM:601152 |
| Blepharophimosis With Ptosis, Syndactyly, And Short Stature |
|
Anosmia, Wide nasal bridge |
OMIM:210745 |
| Hypogonadotropic Hypogonadism 15 With Or Without Anosmia |
|
Anosmia |
OMIM:614880 |
| Refsum Disease, Classic |
|
Anosmia, Ataxia |
OMIM:266500 |
| Indifference To Pain, Congenital, Autosomal Recessive |
|
Anosmia, Hyposmia |
OMIM:243000 |
| Blepharophimosis-Ptosis-Esotropia-Syndactyly-Short Stature Syndrome |
|
Anosmia |
ORPHA:2057 |
| Bleeding Disorder, Platelet-Type, 17 |
|
Impaired epinephrine-induced platelet aggregation, Myelofibrosis, Macrothrombocytopenia, Increase... |
OMIM:187900 |
| Ventricular Extrasystoles With Syncopal Episodes-Perodactyly-Robin Sequence Syndrome |
|
Abnormality of the sense of smell |
ORPHA:3201 |
| Hydrolethalus |
|
Abnormality of the sense of smell, Agenesis of corpus callosum |
ORPHA:2189 |
| Young-Onset Parkinson Disease |
|
Gait imbalance, Hyposmia, Impaired social interactions |
ORPHA:2828 |
| Solitary Median Maxillary Central Incisor |
|
Choanal atresia, Midnasal stenosis, Anosmia, Pyriform aperture stenosis, Abnormal nasopharynx mor... |
OMIM:147250 |
| Marcus-Gunn Syndrome |
|
Abnormality of the sense of smell, Choanal atresia |
ORPHA:91412 |
| Spherocytosis, Type 5 |
|
Hemolytic anemia, Reticulocytosis, Abnormal platelet count, Abnormal leukocyte count, Splenomegal... |
OMIM:612690 |
| Brachytelephalangy-Dysmorphism-Kallmann Syndrome |
|
Abnormal nostril morphology, Anosmia, Short nose |
ORPHA:1295 |
| Kallmann Syndrome With Spastic Paraplegia |
|
Anosmia, Ataxia |
OMIM:308750 |
| Barth Syndrome |
|
Recurrent bronchitis, Gait disturbance, Abnormal mitochondrial morphology |
OMIM:302060 |
| Mitochondrial Phosphate Carrier Deficiency |
|
Abnormal mitochondrial shape |
OMIM:610773 |
| Congenital Disorder Of Glycosylation, Type Iig |
|
Anemia, Camptodactyly, Osteopenia, Giant platelets, Thrombocytopenia |
OMIM:611209 |
| Hypogonadotropic Hypogonadism 13 With Or Without Anosmia |
|
Anosmia |
OMIM:614842 |
| Hypogonadotropic Hypogonadism 25 With Anosmia |
|
Anosmia |
OMIM:618841 |
| Hypogonadotropic Hypogonadism 8 With Or Without Anosmia |
|
Anosmia, Azoospermia |
OMIM:614837 |
| Hypogonadotropic Hypogonadism 10 With Or Without Anosmia |
|
Anosmia |
OMIM:614839 |
| Bardet-Biedl Syndrome 17 |
|
Anosmia, Hyposmia |
OMIM:615994 |
| Ciliary Dyskinesia, Primary, 1 |
|
Recurrent bronchitis, Nasal polyposis, Chronic rhinitis, Anosmia, Absent outer dynein arms |
OMIM:244400 |
| Isolated Follicle Stimulating Hormone Deficiency |
|
Abnormal sperm morphology, Oligospermia, Azoospermia, Anosmia |
ORPHA:52901 |
| Hypogonadotropic Hypogonadism 23 With Or Without Anosmia |
|
Abnormality of the sense of smell, Azoospermia |
OMIM:228300 |
| Paragangliomas 1 |
|
Glomus jugular tumor, Elevated circulating catecholamine level, Glomus tympanicum paraganglioma, ... |
OMIM:168000 |
| Johnson Neuroectodermal Syndrome |
|
Bulbous nose, Anosmia, Choanal atresia |
ORPHA:2316 |
| Refsum Disease |
|
Anosmia, Ataxia |
ORPHA:773 |
| Dystonia-Aphonia Syndrome |
|
Unsteady gait, Gait disturbance, Abnormal mitochondrial shape |
ORPHA:412217 |
| Bernard-Soulier Syndrome |
|
Decreased platelet glycoprotein Ib-IX-V, Macrothrombocytopenia, Impaired ristocetin-induced plate... |
ORPHA:274 |
| Paragangliomas 3 |
|
Glomus jugular tumor, Elevated circulating catecholamine level, Chemodectoma, Paraganglioma, Extr... |
OMIM:605373 |
| Lathosterolosis |
|
Anisopoikilocytosis, Hepatosplenomegaly, Osteoporosis, Schistocytosis, Pathologic fracture, Incre... |
OMIM:607330 |
| Johnson Neuroectodermal Syndrome |
|
Choanal stenosis, Anosmia |
OMIM:147770 |
| Superficial Siderosis |
|
Dysdiadochokinesis, Progressive gait ataxia, Limb ataxia, Ataxia, Dysmetria, Partial anosmia, Ano... |
ORPHA:247245 |
| Muscular Dystrophy, Congenital Hearing Loss, And Ovarian Insufficiency Syndrome |
|
Loss of ambulation, Mitochondrial hypertrophy |
OMIM:619518 |
| Kallmann Syndrome |
|
Ataxia, Anosmia, Hyposmia, Gait disturbance |
ORPHA:478 |
| Hypogonadotropic Hypogonadism 22 With Or Without Anosmia |
|
Anosmia |
OMIM:616030 |
| Optic Atrophy-Ataxia-Peripheral Neuropathy-Global Developmental Delay Syndrome |
|
Gait ataxia, Delayed speech and language development, Abnormal mitochondrial shape, Ataxia |
ORPHA:543470 |
| Takenouchi-Kosaki Syndrome |
|
Thrombocytopenia, Camptodactyly, Increased mean platelet volume |
OMIM:616737 |
| Hypogonadotropic Hypogonadism 12 With Or Without Anosmia |
|
Anosmia |
OMIM:614841 |
| Cardiomyopathy-Hypotonia-Lactic Acidosis Syndrome |
|
Abnormality of the mitochondrion |
ORPHA:91130 |
| Hereditary Leiomyomatosis And Renal Cell Cancer |
|
Decreased fumarate hydratase activity |
OMIM:150800 |
| Friedreich Ataxia |
|
Gait ataxia, Decreased pyruvate carboxylase activity, Limb ataxia, Ataxia, Diabetes mellitus |
OMIM:229300 |
| 8Q21.11 Microdeletion Syndrome |
|
Underdeveloped nasal alae, Abnormality of the sense of smell, Wide nose |
ORPHA:284160 |
| Parkinson Disease 8, Autosomal Dominant |
|
Hyposmia |
OMIM:607060 |
| Septo-Optic Dysplasia Spectrum |
|
Anosmia, Agenesis of corpus callosum |
ORPHA:3157 |
| Acro-Renal-Mandibular Syndrome |
|
Abnormality of the sense of smell |
ORPHA:958 |
| Hereditary Late-Onset Parkinson Disease |
|
Akinesia, Shuffling gait, Hyposmia |
ORPHA:411602 |
| Congenital Hypothyroidism |
|
Anosmia, Depressed nasal ridge |
ORPHA:442 |
| Neuropathy, Hereditary Sensory And Autonomic, Type Viii |
|
Hyposmia |
OMIM:616488 |
| Methylmalonic Aciduria And Homocystinuria, Cbld Type |
|
Decreased methylmalonyl-CoA mutase activity, Lethargy, Spastic ataxia |
OMIM:277410 |
| Progressive External Ophthalmoplegia-Myopathy-Emaciation Syndrome |
|
Decreased mitochondrial number |
ORPHA:352447 |
| Campomelic Dysplasia |
|
Depressed nasal bridge, Abnormality of the sense of smell |
ORPHA:140 |
| Mff-Related Encephalopathy Due To Mitochondrial And Peroxisomal Fission Defect |
|
Abnormal nonverbal communicative behavior, Abnormal mitochondrial shape |
ORPHA:485421 |
| Pure Autonomic Failure |
|
Abnormality of circulating catecholamine level |
ORPHA:441 |
| Methylmalonic Aciduria, Cblb Type |
|
Decreased methylmalonyl-CoA mutase activity, Failure to thrive, Lethargy |
OMIM:251110 |
| Methylmalonic Aciduria, Cbla Type |
|
Decreased methylmalonyl-CoA mutase activity, Failure to thrive, Lethargy |
OMIM:251100 |
| Mitochondrial Complex I Deficiency, Nuclear Type 29 |
|
Decreased activity of mitochondrial complex I, Mitochondrial swelling |
OMIM:618250 |
| Peripheral Neuropathy-Myopathy-Hoarseness-Hearing Loss Syndrome |
|
Mitochondrial swelling |
ORPHA:397744 |
| Holoprosencephaly |
|
Absent nares, Aplasia/Hypoplasia involving the nose, Depressed nasal ridge, Hyposmia, Anosmia, An... |
ORPHA:2162 |
| Fatal Infantile Lactic Acidosis With Methylmalonic Aciduria |
|
Abnormal mitochondrial shape, Choreoathetosis, Decreased activity of mitochondrial complex III, D... |
ORPHA:17 |
| 8P11.2 Deletion Syndrome |
|
Anosmia, Depressed nasal bridge, Azoospermia |
ORPHA:251066 |
| Hyposmia-Nasal And Ocular Hypoplasia-Hypogonadotropic Hypogonadism Syndrome |
|
Absent nares, Single naris, Anosmia, Hyposmia |
ORPHA:2250 |
| Intellectual Developmental Disorder With Impaired Language And Dysmorphic Facies |
|
Delayed speech and language development, Difficulty walking, Hyposmia |
OMIM:618653 |
| Trichohepatoenteric Syndrome 1 |
|
Thrombocytosis, Increased mean platelet volume, Splenomegaly |
OMIM:222470 |
| Macrothrombocytopenia-Lymphedema-Developmental Delay-Facial Dysmorphism-Camptodactyly Syndrome |
|
Thrombocytopenia, Flexion contracture, Camptodactyly, Increased mean platelet volume |
ORPHA:487796 |
| Kallmann Syndrome-Heart Disease Syndrome |
|
Partial anosmia, Total anosmia |
ORPHA:2326 |
| Syndromic Diarrhea |
|
Splenomegaly, Hypoplasia of the thymus, Lymphopenia, Thrombocytosis, Increased mean platelet volume |
ORPHA:84064 |
| Moebius Syndrome |
|
Abnormality of the sense of smell |
ORPHA:570 |
| Congenital Disorder Of Glycosylation, Type Iif |
|
Thrombocytopenia, Neutropenia, Decreased platelet glycoprotein Ib, Macrothrombocytopenia |
OMIM:603585 |
| Combined Oxidative Phosphorylation Deficiency 19 |
|
Mitochondrial swelling |
OMIM:615595 |
| Meningioma |
|
Abnormality of the sense of smell, Difficulty walking, Ataxia |
ORPHA:2495 |
| Glycogen Storage Disease With Severe Cardiomyopathy Due To Glycogenin Deficiency |
|
Increased mitochondrial number |
ORPHA:263297 |
| Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease |
|
Anosmia, Ataxia |
OMIM:609136 |
| Car T Cell Therapy-Associated Cytokine Release Syndrome |
|
Increased circulating interferon-gamma concentration, Increased circulating interleukin 6 concent... |
ORPHA:542323 |
| Amoebiasis Due To Free-Living Amoebae |
|
Ataxia, Hyposmia |
ORPHA:68 |
| Waardenburg Syndrome, Type 2E |
|
Anosmia |
OMIM:611584 |
| Sialuria |
|
Abnormality of the mitochondrion, Wide nasal bridge, Expressive language delay |
ORPHA:3166 |
| Hypogonadotropic Hypogonadism 26 With Or Without Anosmia |
|
Anosmia |
OMIM:619718 |
| Wilson Disease |
|
Hyposmia |
OMIM:277900 |
| Occipital Horn Syndrome |
|
Abnormality of the sense of smell |
ORPHA:198 |
| Bosma Arhinia Microphthalmia Syndrome |
|
Anosmia, Aplasia of the nose, Choanal atresia |
OMIM:603457 |
| Waardenburg Syndrome, Type 4C |
|
Anosmia |
OMIM:613266 |
| Leopard Syndrome 1 |
|
Depressed nasal ridge, Hyposmia |
OMIM:151100 |
| Methylmalonic Aciduria And Homocystinuria, Cblc Type |
|
Decreased methylmalonyl-CoA mutase activity, Failure to thrive, Lethargy |
OMIM:277400 |
| Mitochondrial Dna-Associated Leigh Syndrome |
|
Gait ataxia, Failure to thrive, Abnormality of Krebs cycle metabolism, Ataxia |
ORPHA:255210 |
| Mitochondrial Neurogastrointestinal Encephalomyopathy |
|
Abnormality of the mitochondrion |
ORPHA:298 |
| Charge Syndrome |
|
Depressed nasal bridge, Anosmia, Choanal atresia |
ORPHA:138 |
| Aregenerative Anemia |
|
Abnormality of interleukin secretion |
ORPHA:101096 |
| Lacrimoauriculodentodigital Syndrome |
|
Anosmia, Choanal atresia |
ORPHA:2363 |
| Friedreich Ataxia 2 |
|
Diabetic ketoacidosis, Decreased pyruvate carboxylase activity, Ataxia |
OMIM:601992 |
| Peroxisome Biogenesis Disorder 2A (Zellweger) |
|
Abnormality of the mitochondrion |
OMIM:214110 |
| Autosomal Dominant Progressive External Ophthalmoplegia |
|
Gait ataxia, Gait disturbance, Abnormality of the mitochondrion, Ataxia |
ORPHA:254892 |
| Von Hippel-Lindau Disease |
|
Pancreatic endocrine tumor, Elevated circulating catecholamine level, Pancreatic islet cell adeno... |
ORPHA:892 |
| Charge Syndrome |
|
Anosmia, Choanal atresia |
OMIM:214800 |
| Parkinson Disease 6, Autosomal Recessive Early-Onset |
|
Bradykinesia |
OMIM:605909 |
