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Summary Literature (1)
DOID:0110878 - holoprosencephaly 5

Disease Ontology Definition:A holoprosencephaly that has_material_basis_in heterozygous mutation in the ZIC2 gene on chromosome 13q32.

Synonyms: HPE5,

Xenbase Genes : zic2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012322 - holoprosencephaly 5


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)