hereditary spastic paraplegia 12 (Q32142578)

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hereditary spastic paraplegia that has material basis in mutation in the RTN2 gene on chromosome 19q13
  • autosomal dominant spastic paraplegia 12
  • SPG12
  • autosomal dominant spastic paraplegia type 12
  • SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT; SPG12
  • SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT
  • hereditary spastic paraplegia type 12
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Language Label Description Also known as
English
hereditary spastic paraplegia 12
hereditary spastic paraplegia that has material basis in mutation in the RTN2 gene on chromosome 19q13
  • autosomal dominant spastic paraplegia 12
  • SPG12
  • autosomal dominant spastic paraplegia type 12
  • SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT; SPG12
  • SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT
  • hereditary spastic paraplegia type 12

Statements

instance of
rare disease
0 references
class of disease
0 references

Identifiers

Mondo ID
MONDO_0011489
0 references
 
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