| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant. (Human Disease Ontology, DOID_2383) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0003265 |
| Similar Terms | |
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1 genes associated with the neonatal hyperbilirubinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| GPX1 | glutathione peroxidase 1 |
