Leydig Cell Hypoplasia Type Ii

Leydig 细胞发育不全型 II(来自翻译大模型)

别称:

46,xy Disorder of Sex Developement Due to Partial Luteinizing Hormone Resistance

Leydig Cell Hypoplasia Due to Partial Luteinizing Hormone Receptor Inactivation

46,xy Disorder of Sex Developement Due to Partial Lh Receptor Inactivation

Leydig Cell Hypoplasia Due to Partial Luteinizing Hormone Resistance

46,xy Disorder of Sex Developement Due to Partial Lh Resistance

Leydig Cell Hypoplasia Due to Partial Lh Receptor Inactivation

46,xy Dsd Due to Partial Luteinizing Hormone Resistance

Leydig Cell Hypoplasia Due to Partial Lh Resistance

46,xy Dsd Due to Partial Lh Receptor Inactivation

46,xy Dsd Due to Partial Lh Resistance

Leydig Cell Hypoplasia, Type Ii

加入收藏

基础信息

疾病表征

基因 & 突变

靶点药物

疾病模型

文献报道

Leydig 细胞发育不全型 II，也称为部分黄体生成素抵抗导致的 46,xy 性发育障碍，与 Leydig 细胞发育不全型 I 和 Leydig 细胞发育不全有关。与 Leydig 细胞发育不全型 II 关联的重要基因是 LHCGR（黄体生成素/促性腺激素受体），其相关通路/超级通路包括 G 蛋白信号传导_Rap2B 调节通路和激素配体结合受体。相关表型包括 caspase 3/7 活性降低和肝脏/胆道系统。

查看原文参与反馈