Variant ABeta2M amyloidosis

MONDO:0017810

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.

Also known as: autosomal dominant beta2-microglobulinic amyloidosis

3 clinical trials for this condition and its sub-types, 0 tagged with Variant ABeta2M amyloidosis itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary amyloidosis (79) ↑ ABeta2M amyloidosis (34)

Including sub-types (3) Tagged with Variant ABeta2M amyloidosis (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.