MeSH 搜索器

Diabetes Insipidus, Nephrogenic

A genetic or acquired polyuric disorder characterized by persistent hypotonic urine and HYPOKALEMIA. This condition is due to renal tubular insensitivity to VASOPRESSIN and failure to reduce urine volume. It may be the result of mutations of genes encoding VASOPRESSIN RECEPTORS or AQUAPORIN-2; KIDNEY DISEASES; adverse drug effects; or complications from PREGNANCY.
推出的年份: 1995
副标题
树号: C12.050.351.968.419.135.500, C12.200.777.419.135.500, C12.950.419.135.500
MeSH 单一 ID: D018500
进入的组:
  • Nephrogenic Diabetes Insipidus
  • Nephrogenic Diabetes Insipidus, Type II
  • Diabetes Insipidus, Nephrogenic, Type II
  • Diabetes Insipidus, Nephrogenic, Autosomal
  • Congenital Nephrogenic Diabetes Insipidus
  • Nephrogenic Diabetes Insipidus, Type I
  • Diabetes Insipidus, Nephrogenic, Type 1
  • Diabetes Insipidus, Nephrogenic, Type I
  • Diabetes Insipidus, Nephrogenic, X-Linked
  • Acquired Nephrogenic Diabetes Insipidus
  • ADH-Resistant Diabetes Insipidus
  • Vasopressin-Resistant Diabetes Insipidus
  • Diabetes Insipidus Renalis
早前的内容:
  • Diabetes Insipidus (1966-1994)

留言 (0)

沒有登入
gif