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"

6 matching diseasesClear search ×

OBSOLETE: Secondary acute transverse myelitis

OBSOLETE: Disease-associated transverse myelitis

ORPHA:139420

Acute transverse myelitis

ORPHA:139417

Idiopathic acute transverse myelitis

ORPHA:139423

OBSOLETE: Familial juvenile hyperuricemic nephropathy type 1

OBSOLETE: Familial juvenile gouty nephropathy · OBSOLETE: UMOD-associated familial juvenile hyperuricemic nephropathy

ORPHA:209886

OBSOLETE: Metabolic disease associated with ocular features

ORPHA:98710

OBSOLETE: Vitiligo-associated autoimmune disease

ORPHA:247871