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"

9 matching diseasesClear search ×

X-linked reticulate pigmentary disorder

Familial cutaneous amyloidosis · PDR

ORPHA:85453

AA amyloidosis

Inflammatory amyloidosis · Reactive amyloidosis

ORPHA:85445

AH amyloidosis

Heavy chain amyloidosis

ORPHA:442582

AL amyloidosis

Light-chain amyloidosis

ORPHA:85443

Amyloidosis

ORPHA:69

Familial primary localized cutaneous amyloidosis

FPLCA

ORPHA:353220

Lichen amyloidosis

Amyloid lichen · Lichen amyloidosus

ORPHA:49804

Nodular cutaneous amyloidosis

PLCNA · Primary localized cutaneous nodular amyloidosis

ORPHA:137810

Primary cutaneous amyloidosis

PLCA · Primary localized cutaneous amyloidosis

ORPHA:137807