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Disease Ontology Browser
holoprosencephaly 3 (DOID:0110875)
Alliance: disease page
Synonyms: HLP3; HPE3
Alt IDs: OMIM:142945, MESH:C564181
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the SHH gene on chromosome 7q36.

Disease References using Mouse Models (3)

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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last database update
02/13/2024
MGI 6.23
The Jackson Laboratory