hereditary spastic paraplegia 3A (Q32142983)

From Wikidata
Jump to navigation Jump to search
hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has material basis in mutation in the ATL1 gene on chromosome 14q22
  • FSP1
  • autosomal dominant spastic paraplegia 3
  • strumpell disease
  • autosomal dominant spastic paraplegia type 3
  • autosomal dominant familial spastic paraplegia 1
  • SPG3A
  • Familial Spastic Paraplegia, Autosomal Dominant, 1
  • Spg3
  • hereditary spastic paraplegia type 3A
  • SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A
  • StrC<mpell disease
  • SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT
  • Strümpell disease
edit
Language Label Description Also known as
English
hereditary spastic paraplegia 3A
hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has material basis in mutation in the ATL1 gene on chromosome 14q22
  • FSP1
  • autosomal dominant spastic paraplegia 3
  • strumpell disease
  • autosomal dominant spastic paraplegia type 3
  • autosomal dominant familial spastic paraplegia 1
  • SPG3A
  • Familial Spastic Paraplegia, Autosomal Dominant, 1
  • Spg3
  • hereditary spastic paraplegia type 3A
  • SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A
  • StrC<mpell disease
  • SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT
  • Strümpell disease

Statements

instance of
rare disease
0 references
class of disease
0 references
NCI Thesaurus ID
C142893
0 references

Identifiers

Mondo ID
MONDO_0008437
0 references
 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    Retrieved from "https://www.wikidata.org/w/index.php?title=Q32142983&oldid=2087293475"