familial male-limited precocious puberty. Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Familial male limited precocious puberty (FMPP) is a gonadotropin-independent familial form of male-limited precocious puberty, generally presenting between 2-5 years of age as accelerated growth, early development of secondary sexual characteristics and reduced adult height. (Orphanet Rare Disease Ontology, Orphanet_3000)
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Genes

1 genes associated with the disease familial male-limited precocious puberty. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
LHCGR luteinizing hormone/choriogonadotropin receptor