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中文Leydig Cell Hypoplasia, Type I (LHR)
睾丸间质细胞发育不良I型(来自ICD-11)
别称:
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 细胞发育不全，类型 I，也称为促黄体生成素抵抗，女性，与 Leydig 细胞发育不全类型 II 和男性特异的早熟性性腺功能减退症有关。与 Leydig 细胞发育不全，类型 I 相关的重要基因是 LHCGR（促黄体生成素/绒毛膜促性腺激素受体）。附属组织包括乳腺和睾丸。
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