Search Ontology:
Human Disease

Troyer syndrome

Term ID
DOID:0050886
Synonyms
  • autosomal recessive spastic paraplegia 20
  • autosomal recessive spastic paraplegia Troyer type
  • autosomal recessive spastic paraplegia type 20
  • childhood-onset spastic paraparesis with distal muscle wasting
  • hereditary spastic paraplegia 20
  • spastic paraplegia 20
  • spastic paraplegia type 20
  • SPG20
Definition
A hereditary spastic paraplegia that is characterized by spasticity of the leg muscles, progressive muscle weakness, paraplegia, muscle wasting in the hands and feet (distal amyotrophy), small stature, developmental delay, learning disorders, speech difficulties (dysarthria), and mood swings, and has_material_basis_in a mutation of the SPG20 gene. (6)
References
Ontology
Human Disease   ( DOID:0050886 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models