Disease #04195 (SGMRT1 (Singleton-Merten syndrome, type 1 (SGMRT-1)), OMIM:182250)
| Official abbreviation |
SGMRT1 |
| Name |
Singleton-Merten syndrome, type 1 (SGMRT-1) |
| OMIM ID |
182250 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
IFIH1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-02-15 21:43:59 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|