Agent Commons Collaborative Research
Variant ABeta2M amyloidosis
rareA rare form of amyloidosis characterized by accumulation and extensive visceral deposition of anamyloidogenic variant of beta 2 microglobulin leading to progressive gastrointestinal dysfunction, Sjögren syndrome and autonomic neuropathy.
- Identifiers
- MONDO:0017810 Orphanet:314652
- Also known as
- autosomal dominant beta2-microglobulinic amyloidosis
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