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 ×

Spastic paraplegia type 2

SPG2 · Spastic gait type 2

ORPHA:99015

Autosomal spastic paraplegia type 58

SPAX2 · Autosomal spastic ataxia type 2

ORPHA:397946

Spastic paraplegia type 7

SPG7

ORPHA:99013