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Summary Literature (0)
DOID:0110880 - holoprosencephaly 4


Disease Ontology Definition:A holoprosencephaly that has_material_basis_in heterozygous mutation in the TGIF gene on chromosome 18p11.

Synonyms: HPE4

In OMIM:
OMIM:142946 - HOLOPROSENCEPHALY 4; HPE4

In Mondo Disease Ontology:
MONDO:0007734 - holoprosencephaly 4

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

Xenbase Genes : tgif1

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