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Echinobase
Summary Literature (0)
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,

Echinobase Genes :


OMIM:
MIM:609637 - holoprosencephaly 5; hpe5

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)