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Disease association ontology term - MONDO:0014557 - ataxia - oculomotor apraxia type 4

Term summary

ID
MONDO:0014557
Name
ataxia - oculomotor apraxia type 4
Ontology or CV name
Disease association
Definition
Any oculomotor apraxia or related oculomotor disease in which the cause of the disease is a mutation in the PNKP gene.

Parents

Annotation

Disease association

MONDO:0014557 - ataxia - oculomotor apraxia type 4

References:

Genes: