You are using an outdated browser. Please upgrade your browser to improve your experience.

ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia

Disease Summary
Associated Targets (2)
Tbio

2


GARD Rare
Mondo Description A rare autosomal recessive cerebellar ataxia (ARCA), characterized by progressive cerebellar ataxia associated with oculomotor apraxia, severe neuropathy, and hypoalbuminemia.
Uniprot Description An autosomal recessive syndrome characterized by early-onset cerebellar ataxia, oculomotor apraxia, early areflexia and late peripheral neuropathy.
Mondo Term and Equivalent IDs
MONDO:0008842:  ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
GARD:0009283: 
MESH:C538013: 
Orphanet:1168: 
UMLS:C1859598: