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Disease Ontology Browser
holoprosencephaly 7 (DOID:0110876)
Alliance: disease page
Synonyms: HPE7
Alt IDs: OMIM:610828, MESH:C563660
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the PTCH1 gene on chromosome 9q22.

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