Agent Commons Collaborative Research

Spastic ataxia 4

rare

Any autosomal recessive spastic ataxia in which the cause of the disease is a mutation in the MTPAP gene.

Identifiers
MONDO:0013354 OMIM:613672Orphanet:254343
Causal genes
MTPAP
Part of
Autosomal recessive spastic ataxiaMitochondrial oxidative phosphorylation disorder
Also known as
autosomal recessive spastic ataxia - optic atrophy - dysarthria · autosomal recessive spastic ataxia 4 · autosomal recessive spastic ataxia caused by mutation in MTPAP · autosomal recessive spastic ataxia type 4 · MTPAP autosomal recessive spastic ataxia

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