female reproductive system disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A reproductive system disease that impairs the ability to reproduce and is located in the uterus, vagina, cervix, ovaries or fallopian tubes. (Human Disease Ontology, DOID_229)
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10 genes involed in the disease female reproductive system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
BMP15 bone morphogenetic protein 15
DIAPH2 diaphanous-related formin 2
FIGLA folliculogenesis specific basic helix-loop-helix
FMR1 fragile X mental retardation 1
FOXL2 forkhead box L2
HFM1 HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae)
NOBOX NOBOX oogenesis homeobox
NR5A1 nuclear receptor subfamily 5, group A, member 1
POF1B premature ovarian failure, 1B
STAG3 stromal antigen 3