Rare Disease Library

AApoAI amyloidosis

Apolipoprotein A-I amyloidosis · Familial amyloid nephropathy due to apolipoprotein A-I variant

AA amyloidosis

Inflammatory amyloidosis · Reactive amyloidosis

AApoAII amyloidosis

Apolipoprotein A-II amyloidosis · Familial amyloid nephropathy due to apolipoprotein A-II variant

AApoAIV amyloidosis

Apolipoprotein A-IV amyloidosis

ABri amyloidosis

Familial dementia, British type

ACys amyloidosis

CST3-related amyloidosis · Cystatin amyloidosis

ADan amyloidosis

Familial dementia, Danish type

AFib amyloidosis

Familial amyloid nephropathy due to fibrinogen A alpha-chain variant · Fibrinogen A alpha-chain amyloidosis

AGel amyloidosis

Familial amyloid polyneuropathy type IV · Familial amyloidosis, Finnish type

AH amyloidosis

Heavy chain amyloidosis

AL amyloidosis

Light-chain amyloidosis

ALys amyloidosis

Familial amyloid nephropathy due to lysozyme variant · Familial renal amyloidosis due to lysozyme variant

Amyloidosis

Apolipoprotein A-I deficiency

ApoA-I deficiency · Familial apoA-I deficiency

Hereditary ATTR amyloidosis

Familial TTR-related amyloidosis · Familial transthyretin-related amyloidosis

ITM2B amyloidosis

ITM2B-related amyloidosis · ITM2B-related cerebral amyloid angiopathy

NAD(P)HX epimerase deficiency

Apolipoprotein A-I binding protein deficiency

PrP systemic amyloidosis

Prion protein systemic amyloidosis · Chronic diarrhea with hereditary sensory and autonomic neuropathy