Disease #02851 (DFNB48 (deafness, autosomal recessive, type 48 (DFNB48)), OMIM:609439)
Official abbreviation |
DFNB48 |
Name |
deafness, autosomal recessive, type 48 (DFNB48) |
OMIM ID |
609439 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
8 |
Phenotype entries for this disease |
8 |
Associated with 1 gene |
CIB2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2020-11-11 09:54:01 +01:00 (CET) |
Individuals
|