Disease #04219 (DFNA65 (deafness, autosomal dominant, type 65 (DFNA-65)), OMIM:616044)
| Official abbreviation |
DFNA65 |
| Name |
deafness, autosomal dominant, type 65 (DFNA-65) |
| OMIM ID |
616044 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
TBC1D24 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-03-07 14:59:25 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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