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Echinobase
Summary Literature (0)
DOID:0050754 - ataxia with oculomotor apraxia type 1


Disease Ontology Definition:n_a

Synonyms:

Echinobase Genes : aptx


OMIM:
MIM:208920 - ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia; eaoh

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive cerebellar ataxia (is_a)