Disease #02596 (DFNA36 (deafness, autosomal dominant, type 36 (DFNA-36)), OMIM:606705)
Official abbreviation |
DFNA36 |
Name |
deafness, autosomal dominant, type 36 (DFNA-36) |
OMIM ID |
606705 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
TMC1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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