(Q32143227)
English
hereditary spastic paraplegia 5A
hereditary spastic paraplegia that is characterized by progressive muscle weakness and paraplegia and has material basis in mutation in the CYP7B1 gene on chromosome 8q12
- SPG5A
- autosomal recessive spastic paraplegia type 5A
- autosomal recessive spastic paraplegia 5A
- Spastic paraplegia type 5B, recessive
- hereditary spastic paraplegia type 5A
- SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE
- SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A
Statements
1 reference
1 reference
1 reference
4 references
1 reference
Identifiers
1 reference
1 reference
1 reference
2 references
1 reference
1 reference
1 reference
1 reference