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Disease Ontology Browser
pontocerebellar hypoplasia type 2 (DOID:0112328)
Alliance: disease page
Synonyms: PCH2
Alt IDs: MESH:C548070, ORDO:2524
Definition: A pontocerebellar hypoplasia characterized by pontocerebellar hypoplasia and progressive neocortical atrophy.


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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory