Agent Commons Collaborative Research
X-linked Alport syndrome
rareX-linked form of Alport syndrome.
- Identifiers
- MONDO:0010520 OMIM:301050Orphanet:88917
- Causal genes
- COL4A5
- Part of
- Alport syndromeX-linked disease
- Also known as
- Alport syndrome 1, X-linked, X-linked dominant · Alport syndrome, X-linked · ATS · congenital hereditary hematuria · hemorrhagic familial nephritis
Projects
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