Hypogonadism Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description A gonadal disease that is characterized by diminished functional activity of the gonads. (Human Disease Ontology, DOID_1924)
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Genes

24 genes involed in the disease Hypogonadism from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Symbol Name Standardized Value
CCDC141 coiled-coil domain containing 141 5.0
AXL AXL receptor tyrosine kinase 5.0
SEMA7A semaphorin 7A, GPI membrane anchor (John Milton Hagen blood group) 5.0
WDR11 WD repeat domain 11 4.0
NSMF NMDA receptor synaptonuclear signaling and neuronal migration factor 4.0
IL17RD interleukin 17 receptor D 4.0
SPRY4 sprouty homolog 4 (Drosophila) 4.0
SOX10 SRY (sex determining region Y)-box 10 4.0
PROKR2 prokineticin receptor 2 4.0
ANOS1 anosmin 1 4.0
SMCHD1 structural maintenance of chromosomes flexible hinge domain containing 1 4.0
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A 4.0
FGFR1 fibroblast growth factor receptor 1 4.0
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone) 4.0
FLRT3 fibronectin leucine rich transmembrane protein 3 4.0
HS6ST1 heparan sulfate 6-O-sulfotransferase 1 4.0
PROK2 prokineticin 2 4.0
NDNF neuron-derived neurotrophic factor 4.0
FEZF1 FEZ family zinc finger 1 4.0
FGF17 fibroblast growth factor 17 4.0
TCF12 transcription factor 12 4.0
FGF8 fibroblast growth factor 8 (androgen-induced) 4.0
CHD7 chromodomain helicase DNA binding protein 7 4.0
DUSP6 dual specificity phosphatase 6 4.0