hereditary spastic paraplegia 23 (Q4664694)

From Wikidata
Jump to navigation Jump to search
hereditary spastic paraplegia that has material basis in variation in the chromosome region 1q24-q32
  • spastic paraplegia type 23
  • Lison syndrome
  • SPG23
  • spastic paraplegia with pigmentary abnormalities
  • Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
  • spastic paraplegia 23
  • SPASTIC PARAPLEGIA 23; SPG23
  • Autosomal recessive spastic paraplegia type 23
  • Spastic Paraparesis, Vitiligo, Premature Graying, Characteristic Facies
  • hereditary spastic paraplegia type 23
edit
Language Label Description Also known as
English
hereditary spastic paraplegia 23
hereditary spastic paraplegia that has material basis in variation in the chromosome region 1q24-q32
  • spastic paraplegia type 23
  • Lison syndrome
  • SPG23
  • spastic paraplegia with pigmentary abnormalities
  • Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome
  • spastic paraplegia 23
  • SPASTIC PARAPLEGIA 23; SPG23
  • Autosomal recessive spastic paraplegia type 23
  • Spastic Paraparesis, Vitiligo, Premature Graying, Characteristic Facies
  • hereditary spastic paraplegia type 23

Statements

instance of
rare disease
0 references
class of disease
0 references

Identifiers

Mondo ID
MONDO_0010046
0 references
 
edit
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  Retrieved from "https://www.wikidata.org/w/index.php?title=Q4664694&oldid=2087124802"