| Dataset | GAD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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) |
| Similar Terms | |
| Downloads & Tools |
4 genes associated with the disease holoprosencephaly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
