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)
|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