Disease #00445 (DFNA39 (deafness, autosomal dominant, type 39, with dentinogenesis (DFNA-39)), OMIM:605594)
| Official abbreviation |
DFNA39 |
| Name |
deafness, autosomal dominant, type 39, with dentinogenesis (DFNA-39) |
| OMIM ID |
605594 |
| 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 12:59:49 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|