Disease #02580 (DFNA22 (deafness, autosomal dominant, type 22 (DFNA-22)), OMIM:606346)
Official abbreviation |
DFNA22 |
Name |
deafness, autosomal dominant, type 22 (DFNA-22) |
OMIM ID |
606346 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
MYO6 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|