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ataxia with oculomotor apraxia type 3

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Uniprot Description An autosomal recessive disease characterized by cerebellar ataxia, oculomotor apraxia, areflexia and peripheral neuropathy.
Mondo Term and Equivalent IDs
MONDO:0014084:  ataxia with oculomotor apraxia type 3
GARD:0013112: 
UMLS:C3554690: