Version May 2024
| Autosomal dominant |
| Benign hereditary chorea |
| Dentatorubral pallidoluysian atrophy |
| Familial dyskinesia with facial myokymia |
| Huntington disease |
| Huntington disease-like types 1 and 2 |
| Idiopathic basal ganglia calcification (Fahr disease) |
| Neurodegenerative disease caused by C9ORF72 repeat expansions |
| Neuroferritinopathy |
| Paroxysmal kinesigenic choreoathetosis |
| Paroxysmal nonkinesigenic dyskinesia |
| Spinocerebellar ataxia types 1, 2, 3, and 17 |
| Autosomal recessive |
| Ataxia with oculomotor apraxia types 1 and 2 |
| Ataxia-telangiectasia |
| Chorea-acanthocytosis |
| Friedreich ataxia |
| Huntington disease-like 3 |
| Neuronal ceroid lipofuscinosis |
| Pantothenate kinase-associated neurodegeneration |
| Phenylketonuria |
| Porphyria |
| Wilson disease |
| X-linked |
| McLeod syndrome |
| Lesch-Nyhan disease |
| Maternal inheritance |
| Mitochondrial disorders |
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