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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,
Echinobase Genes :
MIM:142946 - holoprosencephaly 4; hpe4 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
holoprosencephaly (is_a)