Rare Disease Library

ABetaA21G amyloidosis

ABetaA21G-related amyloidosis · HCHWA, Flemish type

ORPHA:324718

AA amyloidosis

Inflammatory amyloidosis · Reactive amyloidosis

ORPHA:85445

ABeta amyloidosis, Arctic type

ABetaE22G amyloidosis · HCHWA, Arctic type

ORPHA:324723

ABeta amyloidosis, Dutch type

HCHWA, Dutch type · HCHWA-D

ORPHA:100006

ABeta amyloidosis, Iowa type

ABetaD23N amyloidosis · HCHWA, Iowa type

ORPHA:324708

ABeta amyloidosis, Italian type

ABetaE22K amyloidosis · HCHWA, Italian type

ORPHA:324713

ABeta2M amyloidosis

Beta2-microglobulinic amyloidosis

ORPHA:439246

ABetaL34V amyloidosis

ABetaL34V-related amyloidosis · HCHWA, Piedmont type

ORPHA:324703

ABri amyloidosis

Familial dementia, British type

ORPHA:97345

ACys amyloidosis

CST3-related amyloidosis · Cystatin amyloidosis

ORPHA:100008

ADan amyloidosis

Familial dementia, Danish type

ORPHA:97346

AFib amyloidosis

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

ORPHA:93562

AGel amyloidosis

Familial amyloid polyneuropathy type IV · Familial amyloidosis, Finnish type

ORPHA:85448

AH amyloidosis

Heavy chain amyloidosis

ORPHA:442582

AL amyloidosis

Light-chain amyloidosis

ORPHA:85443

ALys amyloidosis

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

ORPHA:93561

Amyloidosis

ORPHA:69

Hereditary amyloidosis with primary renal involvement

Amyloidosis, Ostertag type · Familial amyloid nephropathy

ORPHA:85450

Variant ABeta2M amyloidosis

Autosomal dominant beta2-microglobulinic amyloidosis

ORPHA:314652

Wild type ABeta2M amyloidosis

ABeta2Mwt amyloidosis · Dialysis-related amyloidosis

ORPHA:85446

Wild type ATTR amyloidosis

ATTRwt amyloidosis · ATTRwt-related amyloidosis

ORPHA:330001