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variant ABeta2M amyloidosis
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description 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.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
Orphanet:314652
SCTID:722292000
UMLS:C4302669
UMLS:CN203779
MONDO:0017810
High level summary of knowledge for a disease, including descriptions and datasource references.