MeSH 搜索器

Polycystic Kidney, Autosomal Recessive

A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY.
推出的年份: 1992
副标题
树号: C12.050.351.968.419.403.875.510, C12.200.777.419.403.875.510, C12.950.419.403.875.510, C16.131.077.717.510, C16.320.184.625.510
MeSH 单一 ID: D017044
进入的组:
  • Kidney, Polycystic, Autosomal Recessive
  • Autosomal Recessive Polycystic Kidney Disease
  • Polycystic Kidney and Hepatic Disease 1
  • Polycystic Kidney Disease, Infantile, Type I
  • Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive)
  • Polycystic Kidney Disease, Autosomal Recessive
  • Polycystic Kidney Disease, Infantile, Type 1
  • Autosomal Recessive Polycystic Kidney
  • ARPKD
早前的内容:
  • Kidney, Polycystic (1966-1991)

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