gonadotropin deficiency Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A reduced ability to secrete gonadotropins, which are protein hormones secreted by gonadotrope cells of the anterior pituitary gland, including the hormones follitropin (FSH) and luteinizing hormone (LH). (Human Phenotype Ontology, HP_0008213)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008213
Similar Terms
Downloads & Tools

Genes

4 genes associated with the gonadotropin deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHD7 chromodomain helicase DNA binding protein 7
FGFR1 fibroblast growth factor receptor 1
LHX3 LIM homeobox 3
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E