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MeSH 搜索器

Nephritis, Hereditary

A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE.
推出的年份: 1977
副标题
树号: C12.050.351.875.742, C12.050.351.968.419.570.620, C12.200.706.742, C12.200.777.419.570.620, C12.800.742, C12.950.419.570.620, C16.131.939.742, C17.300.200.517
MeSH 单一 ID: D009394
进入的组:
  • Hereditary Nephritis
  • Nephritis, Familial
  • Familial Nephritis
  • Hereditary Interstitial Pyelonephritis
  • Pyelonephritis, Hereditary Interstitial
  • Hemorrhagic Hereditary Nephritis
  • Nephritis, Hemorrhagic Hereditary
  • Hemorrhagic Familial Nephritis
  • Nephritis, Hemorrhagic Familial
  • Hereditary Hematuria Syndrome
  • Congenital Hereditary Hematuria
  • Hematuria, Congenital Hereditary
  • Hematuric Hereditary Nephritis
  • Nephritis, Hematuric Hereditary
  • Hereditary Familial Congenital Hemorrhagic Nephritis
  • Alport Syndrome, Autosomal Recessive
  • Alport Syndrome, X-Linked
  • Alport Syndrome, X Linked
  • X-Linked Alport Syndrome
  • Alport Syndrome
  • Syndrome, Alport
  • Hematuria-Nephropathy-Deafness Syndrome
  • Hematuria Nephropathy Deafness Syndrome
  • Syndrome, Hematuria-Nephropathy-Deafness
  • Alport's Syndrome
  • Alport Syndrome, Autosomal Dominant

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