reticular hyperpigmentation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased pigmentation of the skin with a netlike (reticular) pattern. (Human Phenotype Ontology, HP_0007588)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007588
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Genes

3 genes associated with the reticular hyperpigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
KRT14 keratin 14, type I
PORCN porcupine homolog (Drosophila)
TERC telomerase RNA component