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Disease Ontology Browser
holoprosencephaly 9 (DOID:0110873)
Alliance: disease page
Synonyms: holoprosencephaly with microphthalmia and first branchial arch anomalies; HPE9; pituitary anomalies with holoprosencephaly-like features
Alt IDs: OMIM:610829, MESH:C563659
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the GLI2 gene on chromosome 2q14.

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
11/19/2024
MGI 6.24 		The Jackson Laboratory