Disease #02338 (DFNB9;AUNB1 (deafness, autosomal recessive, type 9), OMIM:601071)
Official abbreviation |
DFNB9;AUNB1 |
Name |
deafness, autosomal recessive, type 9 |
OMIM ID |
601071 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
14 |
Phenotype entries for this disease |
13 |
Associated with 1 gene |
OTOF |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2025-05-15 09:57:37 +02:00 (CEST) |
Individuals
|