Central precocious puberty Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Central precocious puberty (CPP), also referred to as gonadotropin dependent precocious puberty, is an endocrine-related developmental disease characterized by the onset of pubertal changes, with development of secondary sexual characteristics and accelerated growth and bone maturation, before the normal age of puberty (8 years in girls and 9 years in boys). (Orphanet Rare Disease Ontology, Orphanet_759)
External Link http://www.omim.org/entry/176400
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Genes

1 genes associated with the Central precocious puberty phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
KISS1R KISS1 receptor