congenital hydrocephalus 1 Disease Ontology Browser

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Disease Ontology Browser

congenital hydrocephalus 1 (DOID:0070682)
Alliance: disease page
Alt IDs: OMIM:236600, ORDO:269510, UMLS_CUI:C4546092
Definition: A congenital hydrocephalus that has_material_basis_in homozygous mutation in the CCDC88C gene on chromosome 14q32.

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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