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
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