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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 :
MIM:609637 - holoprosencephaly 5; hpe5 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee