Oligomenorrhea Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Infrequent menses (less than 6 per year or more than 35 days between cycles). (Human Phenotype Ontology, HP_0000876)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D009839
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Genes

1 genes/proteins associated with the disease Oligomenorrhea from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1 2.88009