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LHCGR

luteinizing hormone/choriogonadotropin receptor

gene with protein productOMIM: 1527903 заболевания
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Disease-causing germline mutation(s) (loss of function) in2
Leydig cell hypoplasia due to partial LH resistanceORPHA:96266
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Leydig cell hypoplasia due to complete LH resistanceORPHA:96265
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Герминативная мутация (причина)1
Familial peripheral male-limited precocious pubertyORPHA:3000
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Данные: Orphadata (CC-BY-4.0)