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 ×

Severe early-childhood-onset retinal dystrophy

EOSRD · Early-onset severe retinal dystrophy

ORPHA:364055

Best vitelliform macular dystrophy

BMD · BVMD

ORPHA:1243

Bothnia retinal dystrophy

Västerbotten dystrophy

ORPHA:85128

OBSOLETE: Inherited retinal disorder

OBSOLETE: Retinal dystrophy

ORPHA:71862

OBSOLETE: Syndromic inherited retinal disorder

OBSOLETE: Syndromic retinal dystrophy

ORPHA:519325