Primary Ovarian Insufficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An ovarian disease where ovaries do not produce estrogen despite high levels of circulating gonadotropins in women under 40. (Human Disease Ontology, DOID_5426)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D016649
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Genes

3 genes/proteins associated with the disease Primary Ovarian Insufficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FMR1 fragile X mental retardation 1 2.88009
NR5A1 nuclear receptor subfamily 5, group A, member 1 2.88009
CYP2C19 cytochrome P450, family 2, subfamily C, polypeptide 19 2.88009