hypogonadism Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
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

17 genes involed in the disease hypogonadism from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ANOS1 anosmin 1
CHD7 chromodomain helicase DNA binding protein 7
DUSP6 dual specificity phosphatase 6
FGF17 fibroblast growth factor 17
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FLRT3 fibronectin leucine rich transmembrane protein 3
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
HS6ST1 heparan sulfate 6-O-sulfotransferase 1
IL17RD interleukin 17 receptor D
NSMF NMDA receptor synaptonuclear signaling and neuronal migration factor
PROK2 prokineticin 2
PROKR2 prokineticin receptor 2
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SOX10 SRY (sex determining region Y)-box 10
SPRY4 sprouty homolog 4 (Drosophila)
WDR11 WD repeat domain 11