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Echinobase
Summary Literature (0)
DOID:0110873 - holoprosencephaly 9

Disease Ontology Definition:A holoprosencephaly that has_material_basis_in heterozygous mutation in the GLI2 gene on chromosome 2q14.

Synonyms: HPE9, holoprosencephaly with microphthalmia and first branchial arch anomalies, pituitary anomalies with holoprosencephaly-like features,

Echinobase Genes :


OMIM:
MIM:610829 - holoprosencephaly 9; hpe9

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): holoprosencephaly (is_a)