Autosomal dominant Charcot-Marie-Tooth disease type 2D
|
(Orphanet:99938)
|
Autosomal dominant spastic paraplegia type 17
|
(Orphanet:100998)
|
Autosomal dominant spastic paraplegia type 38
|
(Orphanet:171617)
|
Autosomal recessive spastic paraplegia type 11
|
(Orphanet:2822)
|
Beta-mannosidosis
|
(Orphanet:118)
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Connective tissue disorder due to lysyl hydroxylase-3 deficiency
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(Orphanet:300284)
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Distal hereditary motor neuropathy type 5
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(Orphanet:139536)
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Ehlers-Danlos syndrome, spondylocheirodysplastic type
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(Orphanet:157965)
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Mucopolysaccharidosis type 2, attenuated form
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(Orphanet:217093)
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NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA
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(OMIM:600794)
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