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Summary Literature (0)
DOID:0110881 - holoprosencephaly 1

Disease Ontology Definition:A holoprosencephaly that has_material_basis_in variation in the chromosome region 21q22.3.

Synonyms: HPE1

Xenbase Genes : foxh1.2, foxh1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009349 - holoprosencephaly 1

MIM:
MIM:236100 - HOLOPROSENCEPHALY 1; HPE1

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

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