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Summary Literature (0)
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:

Xenbase Genes : znhit3, ccdc88a


MIM:
MIM:260565 - PEHO SYNDROME; PEHO

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): brain disease (is_a)