Disease #06950 (DFNA78 (deafness, autosomal dominant, type 78), OMIM:619081)
Official abbreviation |
DFNA78 |
Name |
deafness, autosomal dominant, type 78 |
OMIM ID |
619081 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
SLC12A2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2022-08-05 13:48:54 +02:00 (CEST) |
Date last edited |
N/A |
Individuals
|