variant ABeta2M amyloidosis https://www.malacards.org/card/dialysis_related_amyloidosis DOID:0080929 GARD:0021382 Orphanet:314652 UMLS:C4302669 A 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. icd11.foundation:1466418791 MONDO:0017810 MEDGEN:928338 SCTID:722292000 autosomal dominant beta2-microglobulinic amyloidosis ABeta2M amyloidosis hereditary amyloidosis