| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A type of holoprosencephaly in which most of the right and left cerebral hemispheres and lateral ventricles are separated but the most rostral aspect of the telencephalon, the frontal lobes, are fused, especially ventrally. (Human Phenotype Ontology, HP_0006870) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0006870 |
| Similar Terms | |
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1 genes associated with the lobar holoprosencephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| FGFR1 | fibroblast growth factor receptor 1 |
