Details of Disease

General Information of Disease (ID: DISSJZ33)

Disease Name AFib amyloidosis
Synonyms
fibrinogen A alpha-chain amyloidosis; familial amyloid nephropathy due to fibrinogen A alpha-chain variant; hereditary amyloid nephropathy due to fibrinogen A alpha-chain variant; hereditary renal amyloidosis due to fibrinogen A alpha-chain variant
Disease Hierarchy
DIS7BVSW: Familial visceral amyloidosis
DISSJZ33: AFib amyloidosis
Disease Identifiers
MONDO ID
MONDO_0019733
UMLS CUI
C5680267
MedGen ID
1826152
Orphanet ID
93562

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
FGA OTMIHY80 Supportive Autosomal dominant [1]
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References

1 Renal amyloidosis with a frame shift mutation in fibrinogen aalpha-chain gene producing a novel amyloid protein. Blood. 1997 Dec 15;90(12):4799-805.