Disease #02352 (DFNA-11 (deafness, autosomal dominant, type 11 (DFNA-11)), OMIM:601317)
Official abbreviation |
DFNA-11 |
Name |
deafness, autosomal dominant, type 11 (DFNA-11) |
OMIM ID |
601317 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
MYO7A |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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