Disease #00442 (DGI3 (dentinogenesis imperfecta, Shields type III (DGI-3)), OMIM:125500)
| Official abbreviation |
DGI3 |
| Name |
dentinogenesis imperfecta, Shields type III (DGI-3) |
| OMIM ID |
125500 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
DSPP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-07-09 12:54:35 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|