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ENLeydig Cell Hypoplasia, Type I (LHR)
Alias:
Luteinizing Hormone Resistance, Female
Leydig Cell Agenesis
Leydig Cell Hypoplasia Type I
46,xy Disorder of Sex Development Due to Complete Luteinizing Hormone Receptor Inactivation
46,xy Disorder of Sex Development Due to Complete Luteinizing Hormone Resistance
Leydig Cell Hypoplasia Due to Complete Luteinizing Hormone Receptor Inactivation
46,xy Disorder of Sex Development Due to Complete Lh Receptor Inactivation
Leydig Cell Hypoplasia Due to Complete Luteinizing Hormone Resistance
46,xy Dsd Due to Complete Luteinizing Hormone Receptor Inactivation
46,xy Disorder of Sex Development Due to Complete Lh Resistance
Leydig Cell Hypoplasia Due to Complete Lh Receptor Inactivation
Leydig Cell Hypoplasia with Hypergonadotropic Hypogonadism
46,xy Dsd Due to Complete Luteinizing Hormone Resistance
Leydig Cell Hypoplasia with Male Pseudohermaphroditism
46,xy Dsd Due to Complete Lh Receptor Inactivation
46,xy Dsd Due to Complete Lh Resistance
Leydig Cell Hypoplasia
Hypergonadotropic Hypogonadism, Male, Due to Lhcgr Defect
Hypergonadotropic Hypogonadism Male Due to Lhcgr Defect
Leydig Cell Hypoplasia Due to Complete Lh Resistance
Leydig Cell Hypoplasia with Pseudohermaphroditism
Testicular Luteinizing Hormone Resistance
Ovarian Luteinizing Hormone Resistance
Female Luteinizing Hormone Resistance
Leydig Cell Hypoplasia, Complete
Leydig Cell Hypoplasia Complete
Leydig Cell Hypoplasia, Partial
Leydig Cell Hypoplasia Type Ii
Luteinizing Hormone Resistance
Leydig Cell Hypoplasia Partial
Hypoplasia, Leydig Cell
Lhr
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Leydig Cell Hypoplasia, Type I, also known as luteinizing hormone resistance, female, is related to leydig cell hypoplasia type ii and precocious puberty, male-limited. An important gene associated with Leydig Cell Hypoplasia, Type I is LHCGR (Luteinizing Hormone/Choriogonadotropin Receptor). Affiliated tissues include breast and testes.
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MALACARDS
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IF
