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ataxia - oculomotor apraxia type 4

Disease Summary
Associated Targets (1)
Tchem

1


GARD Rare
Mondo Description Any oculomotor apraxia or related oculomotor disease in which the cause of the disease is a mutation in the PNKP gene.
Uniprot Description An autosomal recessive disease characterized by cerebellar ataxia, oculomotor apraxia, areflexia and peripheral neuropathy.
Mondo Term and Equivalent IDs
MONDO:0014557:  ataxia - oculomotor apraxia type 4
EFO:0009016: 
GARD:0013111: 
Orphanet:459033: 
UMLS:C4225397: