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GTR Home > Conditions/Phenotypes > Gonadotropin-independent familial sexual precocity

Gonadotropin-independent familial sexual precocity

Synonyms
Familial Testotoxicosis (subtype); Familial male-limited precocious puberty; Male-Limited Precocious Puberty; Pubertas Praecox; TESTOTOXICOSIS, FAMILIAL; Testotoxicosis
Modes of inheritance
Autosomal dominant inheritance (Orphanet)

Summary

Familial male precocious puberty is a gonadotropin-independent disorder that is inherited in an autosomal dominant, male-limited pattern. Affected males generally exhibit signs of puberty by age 4 years (Shenker et al., 1993). [from OMIM]

Available tests

24 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (24 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: HHG, LCGR, LGR2, LH/CG-R, LH/CGR, LHR, LHRHR, LSH-R, ULG5, LHCGR
    Summary: luteinizing hormone/choriogonadotropin receptor

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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