Disease #04161 (STUT2 (stuttering, familial, persistent, type 2 (STUT-2)), OMIM:609261)
| Official abbreviation |
STUT2 |
| Name |
stuttering, familial, persistent, type 2 (STUT-2) |
| OMIM ID |
609261 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
43 |
| Phenotype entries for this disease |
43 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-12-19 16:17:19 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|