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
|