Autosomal dominant optic atrophy, classic type
|
(Orphanet:98673)
|
Autosomal dominant spastic paraplegia type 3
|
(Orphanet:100984)
|
Autosomal dominant spastic paraplegia type 4
|
(Orphanet:100985)
|
Autosomal dominant spastic paraplegia type 6
|
(Orphanet:100988)
|
Autosomal dominant spastic paraplegia type 8
|
(Orphanet:100989)
|
Charcot-Marie-Tooth disease type 1A
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(Orphanet:101081)
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Charcot-Marie-Tooth disease type 1B
|
(Orphanet:101082)
|
Monomelic amyotrophy
|
(Orphanet:65684)
|
PARKINSON DISEASE 18, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO
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(OMIM:614251)
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PARKINSON DISEASE, LATE-ONSET
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(OMIM:168600)
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Spinocerebellar ataxia type 30
|
(Orphanet:211017)
|