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Summary Literature (4)
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)


In Mondo Disease Ontology:
MONDO:0016296 - holoprosencephaly

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

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

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): congenital nervous system abnormality (is_a), syndrome (is_a)