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Disease Ontology Browser
holoprosencephaly (DOID:4621)
Alliance: disease page
Synonyms: Holoprosencephaly sequence
Alt IDs: ICD10CM:Q04.2, MESH:D016142, NCI:C74988, OMIM:PS236100, ORDO:2162, UMLS_CUI:C0079541
Definition: A congenital nervous system abnormality characterized by failed or incomplete separation of the forebrain early in gestation; it is accompanied by a spectrum of characteristic craniofacial anomalies.

Disease References using Mouse Models (14)
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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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory