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DOID:0080539 - PEHO syndrome
Disease Ontology Definition:A brain disease that is characterized by extreme cerebellar atrophy due to almost total granule neuron loss.
Synonyms:
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
brain disease (is_a)