Alpha-N-acetylgalactosaminidase deficiency type 2
|
(Orphanet:79280)
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Amyotrophic lateral sclerosis type 4
|
(Orphanet:357043)
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Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
|
(Orphanet:100044)
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CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S
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(OMIM:616155)
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CREST syndrome
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(Orphanet:90290)
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MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2
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(OMIM:615157)
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NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA
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(OMIM:608720)
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Neuralgic amyotrophy
|
(Orphanet:2901)
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Spastic paraplegia 64, autosomal recessive
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(OMIM:615683)
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X-linked Charcot-Marie-Tooth disease type 1
|
(Orphanet:101075)
|