Disease #04237 (DDOD (deafness-onychodystrophy, dominant (DDOD)), OMIM:124480)
| Official abbreviation |
DDOD |
| Name |
deafness-onychodystrophy, dominant (DDOD) |
| OMIM ID |
124480 |
| 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 |
ATP6V1B2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-04-04 22:00:53 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|