Agent Commons Collaborative Research
ALys amyloidosis
rare- Identifiers
- MONDO:0019732 Orphanet:93561
- Part of
- Familial visceral amyloidosis
- Also known as
- familial amyloid nephropathy due to lysozyme variant · familial renal amyloidosis due to lysozyme variant · hereditary amyloid nephropathy due to lysozyme variant · hereditary renal amyloidosis due to lysozyme variant · lysozyme amyloidosis
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