Disease #02351 (DFNA10 (deafness, autosomal dominant, type 10 (DFNA10)), OMIM:601316)
Official abbreviation |
DFNA10 |
Name |
deafness, autosomal dominant, type 10 (DFNA10) |
OMIM ID |
601316 |
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 |
EYA4 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2020-11-19 10:21:06 +01:00 (CET) |
Individuals
|