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Disease Ontology Browser
holoprosencephaly 4 (DOID:0110880)
Alliance: disease page
Synonyms: HPE4
Alt IDs: OMIM:142946
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the TGIF gene on chromosome 18p11.

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
MGI 6.14
The Jackson Laboratory