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LHCGR

luteinizing hormone/choriogonadotropin receptor

HCNC Approved Symbol
LHCGR (HGNC:6585)
Genomic Coordinates
2:48,686,774 - 48,755,724 (2p16.3)
Synonyms
LHR, LCGR, LGR2, ULG5, HHG
Disease Associations
This gene is associated with the following 5 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Leydig cell adenoma, somatic, with precocious puberty
176410-
Leydig cell hypoplasia with hypergonadotropic hypogonadism
238320AR
Leydig cell hypoplasia with pseudohermaphroditism
238320AR
Luteinizing hormone resistance, female
238320AR
Precocious puberty, male
176410AD

Diagnosed Cases

3Patients

In total, 3 patients were diagnosed with a variant in the LHCGR gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Advanced bone age
 3 (100.0%)
High serum testosterone level
 2 (66.7%)
Precocious puberty
 2 (66.7%)
Tall stature
 2 (66.7%)
Precocious puberty in males
 1 (33.3%)