abnormal pigmentation of the oral mucosa Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the pigmentation of the mucosa of the mouth. (Human Phenotype Ontology, HP_0100669)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100669
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Genes

4 genes associated with the abnormal pigmentation of the oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FERMT1 fermitin family member 1
LAMA3 laminin, alpha 3
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
STK11 serine/threonine kinase 11