Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
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, Ontobee
Parent(s): brain disease (is_a)