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Disease Ontology Browser
holoprosencephaly (DOID:4621)
Synonyms: Holoprosencephaly sequence (disorder)
Alt IDs: OMIM:142945, OMIM:142946, OMIM:157170, OMIM:236100, OMIM:605934, OMIM:609408, OMIM:609637, OMIM:610828, OMIM:610829, OMIM:614226, ICD10CM:Q04.2, MESH:D016142, NCI:C74988, 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 (11)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory