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"

4 matching diseasesClear search ×

Sporadic porphyria cutanea tarda

Porphyria cutanea tarda type I

ORPHA:443057

Familial porphyria cutanea tarda

Porphyria cutanea tarda type II

ORPHA:443062

Hepatic cutaneous porphyria

ORPHA:659698

Porphyria cutanea tarda

PCT

ORPHA:101330