congenital hydrocephalus 4 Disease Ontology Browser

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Disease Ontology Browser

congenital hydrocephalus 4 (DOID:0070685)
Alliance: disease page
Alt IDs: OMIM:618667, UMLS_CUI:C5231454
Definition: A congenital hydrocephalus that has_material_basis_in heterozygous mutation in the TRIM71 gene on chromosome 3p22.

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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