| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores |
| 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 | |
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8 genes involed in the disease holoprosencephaly from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
