Vaginal Septum Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description a longitudinal or transverse congenital partition within the muscular canal extending from outside of the body to the cervix; usually caused by incomplete fusion of the Mullerian ducts in embryogenesis (Mammalian Phenotype Ontology, MP_0009708)
External Link https://www.disgenet.org/browser/0/1/0/C0431649
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Genes

2 genes associated with the disease Vaginal Septum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
LEP leptin