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Summary Literature (6)
DOID:4621 - holoprosencephaly

Disease Ontology Definition:A congenital nervous system abnormality characterized by failed or incomplete separation of the forebrain early in gestation; it is accompanied by a spectrum of characteristic craniofacial anomalies.

Synonyms: Holoprosencephaly sequence, Holoprosencephaly sequence (disorder),

Xenbase Genes : foxh1.2, six3, gli2, zic2, shh, ptch1, tgif1, cdon, foxh1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0016296 - holoprosencephaly


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): congenital nervous system abnormality (is_a), syndrome (is_a)