Disease #02397 (DFNA13 (deafness, autosomal dominant, type 13 (DFNA-13)), OMIM:601868)
Official abbreviation |
DFNA13 |
Name |
deafness, autosomal dominant, type 13 (DFNA-13) |
OMIM ID |
601868 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
COL11A2 |
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
|