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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

In OMIM:
OMIM:609637 - HOLOPROSENCEPHALY 5; HPE5

In Mondo Disease Ontology:
MONDO:0012322 - holoprosencephaly 5

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : zic2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): holoprosencephaly (is_a)