Disease - Amyloidosis, hereditary systemic 3
- DefinitionA form of hereditary systemic amyloidosis, a disorder characterized by amyloid deposition in multiple tissues resulting in a wide clinical spectrum. AMYLD3 clinical features include amyloid neuropathy, nephropathy, hepatopathy, and cardiomyopathy. Inheritance is autosomal dominant.
- AcronymAMYLD3
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Browse 1 entry- Apolipoprotein A-I · Gene: APOA1 · Homo sapiens (Human) · 267 amino acids · Evidence at protein level · Annotation score: 5/5