|Dataset||HuGE Navigator Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||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. (Human Disease Ontology, DOID_4621)|
|Downloads & Tools|
6 genes associated with the Holoprosencephaly phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.