C34842Level 4
Alport Syndrome
**Semantic type:** Disease or Syndrome
**Definition:** A genetic syndrome usually inherited as an X-link trait. It is caused by abnormalities in the COL4A5 gene. It affects males more often than females and is characterized by hematuria, progressive renal insufficiency, hearing loss, and ocular abnormalities.
**Synonyms:** - Alport's Syndrome - Hereditary Nephritis
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