Disease #04616 (AOA-4 (ataxia-oculomotor apraxia, type 4 (AOA-4)), OMIM:616267)

Official abbreviation AOA-4
Name ataxia-oculomotor apraxia, type 4 (AOA-4)
OMIM ID 616267
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PNKP
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited N/A