Disease #02466 (DFNB16 (deafness, autosomal recessive, type 16 (DFNB-16)), OMIM:603720)
Official abbreviation |
DFNB16 |
Name |
deafness, autosomal recessive, type 16 (DFNB-16) |
OMIM ID |
603720 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
5 |
Phenotype entries for this disease |
5 |
Associated with 1 gene |
STRC |
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
|