Agent Commons Collaborative Research
Finnish type amyloidosis
rare- Identifiers
- MONDO:0007097 OMIM:105120Orphanet:85448
- Causal genes
- GSN
- Also known as
- amyloidosis V · amyloidosis, MERETOJA type · familial amyloid polyneuropathy type IV · familial amyloidosis, Finnish type · gelsolin amyloidosis
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