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Disease Ontology Browser
pontocerebellar hypoplasia type 15 (DOID:0112326)
Alliance: disease page
Synonyms: PCH15
Alt IDs: OMIM:619302
Definition: A pontocerebellar hypoplasia that has_material_basis_in homozygous or compound heterozygous mutation in the CDC40 gene on chromosome 6q21.

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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11/12/2024
MGI 6.24 		The Jackson Laboratory