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DOID:0060264 - pontocerebellar hypoplasia
Disease Ontology Definition:A neurodegenerative disease that is characterized by underdevelopment of the pons and cerebellum.
Synonyms: PCH,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0020135 - pontocerebellar hypoplasia |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
neurodegenerative disease (is_a)