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DOID:0050754 - ataxia with oculomotor apraxia type 1
Disease Ontology Definition:n_a
Synonyms:
Echinobase Genes : aptx
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)