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"

5 matching diseasesClear search ×

X-linked erythropoietic protoporphyria

X-linked dominant erythropoietic protoporphyria · X-linked dominant protoporphyria

ORPHA:443197

Autosomal erythropoietic protoporphyria

EPP

ORPHA:79278

Congenital erythropoietic porphyria

CEP · Günther disease

ORPHA:79277

Erythropoietic porphyria

EPP

ORPHA:659681

Hepatoerythropoietic porphyria

HEP

ORPHA:95159