abnormality of the labia minora Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the labia minora, the folds of skin between the outer labia. (Human Phenotype Ontology, HP_0012880)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012880
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8 genes associated with the abnormality of the labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATIC 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
FGFR2 fibroblast growth factor receptor 2
KAT6B K(lysine) acetyltransferase 6B
NDN necdin, melanoma antigen (MAGE) family member
ORC1 origin recognition complex, subunit 1
SETBP1 SET binding protein 1
SNRPN small nuclear ribonucleoprotein polypeptide N