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"

16 matching diseasesClear search ×

Autosomal spastic paraplegia type 72

SPG72

Autosomal dominant spastic paraplegia type 4

SPG4

Autosomal dominant spastic paraplegia type 6

SPG6

Autosomal dominant spastic paraplegia type 73

SPG73

Autosomal dominant spastic paraplegia type 8

SPG8

Autosomal recessive spastic paraplegia type 70

SPG70

Autosomal recessive spastic paraplegia type 71

SPG71

Autosomal recessive spastic paraplegia type 74

SPG74

Autosomal recessive spastic paraplegia type 75

SPG75

Autosomal recessive spastic paraplegia type 76

SPG76

Autosomal recessive spastic paraplegia type 77

SPG77

Autosomal recessive spastic paraplegia type 78

SPG78

Hereditary spastic paraplegia

Familial spastic paraplegia · HSP

Spastic paraplegia type 2

SPG2 · Spastic gait type 2

Spastic paraplegia type 7

SPG7

X-linked complicated spastic paraplegia type 1

SPG1