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"

17 matching diseasesClear search ×

Autosomal recessive spastic paraplegia type 66

SPG66

Autosomal dominant spastic paraplegia type 4

SPG4

Autosomal dominant spastic paraplegia type 6

SPG6

Autosomal dominant spastic paraplegia type 8

SPG8

Autosomal recessive spastic paraplegia type 45

Autosomal recessive spastic paraplegia type 65 · SPG45

Autosomal recessive spastic paraplegia type 60

SPG60

Autosomal recessive spastic paraplegia type 61

SPG61

Autosomal recessive spastic paraplegia type 62

SPG62

Autosomal recessive spastic paraplegia type 63

SPG63

Autosomal recessive spastic paraplegia type 64

SPG64

Autosomal recessive spastic paraplegia type 67

SPG67

Autosomal recessive spastic paraplegia type 68

SPG68

Autosomal recessive spastic paraplegia type 69

SPG69

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