Disease #06168 (DFNA69 (Deafness, autosomal dominant 69, unilateral or asymmetric), OMIM:616697)
| Official abbreviation |
DFNA69 |
| Name |
Deafness, autosomal dominant 69, unilateral or asymmetric |
| OMIM ID |
616697 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
KITLG |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
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