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Summary Literature (0)
DOID:0110872 - holoprosencephaly 2

Disease Ontology Definition:A holoprosencephaly that has_material_basis_in mutation in the homeobox-containing SIX3 gene on chromosome 2p21.

Synonyms: HPE2,

Xenbase Genes : six3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007999 - holoprosencephaly 2


Other Model Organisms: AGR, 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)