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Summary Literature (0)
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

In OMIM:
OMIM:142945 - HOLOPROSENCEPHALY 3; HPE3

In Mondo Disease Ontology:
MONDO:0007733 - holoprosencephaly 3

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : shh

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): holoprosencephaly (is_a)