Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:208920 - ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH

Xenbase Genes: aptx

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008842 - ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia

Disease Ontology (DO):
DOID:0050754 - early-onset ataxia with oculomotor apraxia and hypoalbuminemia