Disease #00290 (GTS (Gilles de la Tourette syndrome (GTS)), OMIM:137580)
Official abbreviation |
GTS |
Name |
Gilles de la Tourette syndrome (GTS) |
OMIM ID |
137580 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
9 |
Phenotype entries for this disease |
2 |
Associated with 2 genes |
HDC, SLITRK1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-12-20 10:46:12 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|