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"

3 matching diseasesClear search ×

Norrie disease

Atrophia bulborum hereditaria · Episkopi blindness

ORPHA:649

Familial anetoderma

Hereditary anetoderma · Hereditary macular atrophy

ORPHA:228277

Hereditary neutrophilia

ORPHA:279943