Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

12 matching diseasesClear search ×

Amyloidosis cutis dyschromia

Amyloidosis cutis dyschromica

ORPHA:319635

AA amyloidosis

Inflammatory amyloidosis · Reactive amyloidosis

ORPHA:85445

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 ATTR amyloidosis

Familial TTR-related amyloidosis · Familial transthyretin-related amyloidosis

ORPHA:271861