Disease #01011 (DFNA-20;DFNA-26 (deafness, autosomal dominant, type 20/26 (DFNA-20;DFNA-26)), OMIM:604717)
| Official abbreviation |
DFNA-20;DFNA-26 |
| Name |
deafness, autosomal dominant, type 20/26 (DFNA-20;DFNA-26) |
| OMIM ID |
604717 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ACTG1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
