Troyer syndrome (Q3508706)

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gene (13q13.1), which encodes the protein spartin.
  • spastic paraplegia 20 (Troyer syndrome)
  • spastic paraplegia type 20
  • autosomal recessive spastic paraplegia Troyer type
  • autosomal recessive spastic paraplegia 20
  • autosomal recessive spastic paraplegia type 20
  • childhood-onset spastic paraparesis with distal muscle wasting
  • SPG20
  • hereditary spastic paraplegia 20
  • spastic paraplegia 20
  • Spastic Paraplegia, Autosomal Recessive, Troyer Type
  • SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20
  • Spastic paraplegia 20, autosomal recessive
  • Troyer Syndrome
  • Childhood-onset spastic paraparesis-distal muscle wasting syndrome
  • Spastic Paraparesis, Childhood-Onset, With Distal Muscle Wasting
  • Cross-McKusick syndrome
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Language Label Description Also known as
English
Troyer syndrome
gene (13q13.1), which encodes the protein spartin.
  • spastic paraplegia 20 (Troyer syndrome)
  • spastic paraplegia type 20
  • autosomal recessive spastic paraplegia Troyer type
  • autosomal recessive spastic paraplegia 20
  • autosomal recessive spastic paraplegia type 20
  • childhood-onset spastic paraparesis with distal muscle wasting
  • SPG20
  • hereditary spastic paraplegia 20
  • spastic paraplegia 20
  • Spastic Paraplegia, Autosomal Recessive, Troyer Type
  • SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20
  • Spastic paraplegia 20, autosomal recessive
  • Troyer Syndrome
  • Childhood-onset spastic paraparesis-distal muscle wasting syndrome
  • Spastic Paraparesis, Childhood-Onset, With Distal Muscle Wasting
  • Cross-McKusick syndrome

Statements

instance of
rare disease
0 references
class of disease
0 references

Identifiers

Mondo ID
MONDO_0010156
0 references
 
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