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"

2 matching diseasesClear search ×

Familial primary localized cutaneous amyloidosis

FPLCA

ORPHA:353220

Primary cutaneous amyloidosis

PLCA · Primary localized cutaneous amyloidosis

ORPHA:137807