(Q32142563)
English
hereditary spastic paraplegia 11
hereditary spastic paraplegia that has material basis in mutation in the SPG11 gene on chromosome 15q21
- spastic paraplegia-intellectual disability-thin corpus callosum syndrome
- autosomal recessive spastic paraplegia type 11
- autosomal recessive spastic paraplegia complicated with thin corpus callosum
- autosomal recessive spastic paraplegia 11
- Nakamura-Osame syndrome
- SPG11
- autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum
- HSP-TCC
- Spastic Paraplegia, Autosomal Recessive, Complicated, With Thin Corpus Callosum
- hereditary spastic paraplegia type 11
- Spastic Paraplegia, Autosomal Recessive, With Mental Impairment and Thin Corpus Callosum
- SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE
- SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11
Statements
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
4 references
C148317
0 references
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
2 references
1 reference
1 reference
1 reference
1 reference