| Metadata | |
|---|---|
| ID | DOID:0050886 |
| Name | Troyer syndrome |
| 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. http://en.wikipedia.org/wiki/SPG20, http://ghr.nlm.nih.gov/condition/troyer-syndrome, http://ghr.nlm.nih.gov/gene/SPG20, http://omim.org/entry/275900, http://www.orpha.net/consor/cgi-bin//Disease_Search.php?lng=EN&data_id=14711&Disease_Disease_Search_diseaseGroup=spastic-paraplegia&Disease_Disease_Search_diseaseType=Pat&Disease(s)/group%20of%20diseases=Autosomal-recessive-spastic-paraplegia-type-20&title=Autosomal-recessive-spastic-paraplegia-type-20&search=Disease_Search_Simple, https://www.ncbi.nlm.nih.gov/pubmed/20301556 |
| Xrefs | |
| Subsets |
DO_FlyBase_slim DO_rare_slim |
| Synonyms |
autosomal recessive spastic paraplegia 20 [EXACT] autosomal recessive spastic paraplegia Troyer type [EXACT] autosomal recessive spastic paraplegia type 20 [EXACT] childhood-onset spastic paraparesis with distal muscle wasting [EXACT] hereditary spastic paraplegia 20 [EXACT] spastic paraplegia 20 [EXACT] spastic paraplegia type 20 [EXACT] SPG20 [EXACT] |
| Parent Relationships |