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Metadata
ID DOID:0111170
Name autosomal dominant sensory ataxia 1
Definition A hereditary ataxia characterized by gait difficulty and instability especially in dark conditions resulting from sensory loss in the extremities and without cerebellar involvement that has_material_basis_in heterozygous mutations in the RNF170 gene on chromosome 8.
https://www.ncbi.nlm.nih.gov/pubmed/15286160
Xrefs

OMIM:608984

Synonyms

ADSA [EXACT]

SNAX1 [EXACT]

Parent Relationships

is_a hereditary ataxia

is_a autosomal dominant disease

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