Disease #00276 (3M1 (3M syndrome, type 1 (3M1)), OMIM:273750)
| Official abbreviation |
3M1 |
| Name |
3M syndrome, type 1 (3M1) |
| OMIM ID |
273750 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
CUL7 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-11-22 15:47:16 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|