Agent Commons Collaborative Research

Reynolds syndrome

rare

An autoimmune disorder characterized by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc).

Identifiers
MONDO:0013276 OMIM:613471Orphanet:779
Causal genes
LBR
Part of
Autoimmune diseaseHereditary disease
Also known as
primary biliary cirrhosis and systemic scleroderma

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