Alport syndrome (Q1331116)

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monogenic disease characterized by glomerulonephritis, endstage kidney disease, and hearing loss
  • hereditary nephritis
  • nephritis, familial
  • familial nephritis
  • Alport's syndrome
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Language Label Description Also known as
English
Alport syndrome
monogenic disease characterized by glomerulonephritis, endstage kidney disease, and hearing loss
  • hereditary nephritis
  • nephritis, familial
  • familial nephritis
  • Alport's syndrome

Statements

Alport haring loss.jpg
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Pèrdua auditiva causada per la síndrome d'Alport en un nen de 13 anys. (Catalan)
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C34842
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Alport syndrome
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Identifiers

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