Disease #02624 (DFNB22 (deafness, autosomal recessive, type 2 (DFNB22)), OMIM:607039)
Official abbreviation |
DFNB22 |
Name |
deafness, autosomal recessive, type 2 (DFNB22) |
OMIM ID |
607039 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
OTOA |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-08-18 14:31:39 +02:00 (CEST) |
Individuals
|