Rare Disease Library

Spastic paraplegia type 2

SPG2 · Spastic gait type 2

Autosomal dominant spastic paraplegia type 29

SPG29

Autosomal recessive spastic paraplegia type 20

Childhood-onset spastic paraparesis-distal muscle wasting syndrome · SPG20

Autosomal recessive spastic paraplegia type 21

Mast syndrome · SPG21

Autosomal recessive spastic paraplegia type 23

Lison syndrome · SPG23

Autosomal recessive spastic paraplegia type 24

SPG24

Autosomal recessive spastic paraplegia type 25

Autosomal recessive spastic paraplegia-disc herniation syndrome · SPG25

Autosomal recessive spastic paraplegia type 26

GM2 synthase deficiency · SPG26

Autosomal recessive spastic paraplegia type 27

SPG27

Autosomal recessive spastic paraplegia type 28

SPG28

Autosomal spastic paraplegia type 18

SPG18

Autosomal spastic paraplegia type 30

SPG30

Autosomal spastic paraplegia type 58

SPAX2 · Autosomal spastic ataxia type 2

Autosomal spastic paraplegia type 72

SPG72

Hereditary spastic paraplegia

Familial spastic paraplegia · HSP

Kjellin syndrome

Hereditary spastic paraparesis type 15 · Autosomal recessive spastic paraplegia type 15

Spastic paraparesis-cataracts-speech delay syndrome

Fatty acyl-CoA reductase 1 superactivity

Spastic paraparesis-deafness syndrome

Wells-Jankovic syndrome · Spastic paraparesis-hearing loss syndrome

Spastic paraplegia type 7

SPG7

Tropical spastic paraparesis

HAM/TSP · HTLV-1-associated myelopathy/tropical spastic paraparesis

X-linked spastic paraplegia type 16

SPG16

X-linked spastic paraplegia type 34

SPG34