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Disease Ontology Browser
holoprosencephaly 3 (DOID:0110875)
Alliance: disease page
Synonyms: HLP3; HPE3
Alt IDs: OMIM:142945
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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.11
The Jackson Laboratory