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Summary Literature (0)
DOID:0110877 - holoprosencephaly 11


Disease Ontology Definition:A holoprosencephaly that has_material_basis_in heterozygous mutation in the CDON gene on chromosome 11q24.

Synonyms: HPE11,

Xenbase Genes : cdon

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013642 - holoprosencephaly 11


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): holoprosencephaly (is_a)