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DOID:0110875 - holoprosencephaly 3
Disease Ontology Definition:A holoprosencephaly that has_material_basis_in heterozygous mutation in the SHH gene on chromosome 7q36.
Synonyms: HLP3, HPE3,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0007733 - holoprosencephaly 3 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee