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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 - ataxia with oculomotor apraxia type 1