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Disease Ontology Browser
PEHO syndrome (DOID:0080539)
Alliance: disease page
Alt IDs: OMIM:260565, MESH:C536317, ORDO:2836
Definition: A brain disease that is characterized by extreme cerebellar atrophy due to almost total granule neuron loss.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory