Disease #04622 (DFNX2 (deafness, X-linked, type 2 (DFNX-2)), OMIM:304400)
| Official abbreviation |
DFNX2 |
| Name |
deafness, X-linked, type 2 (DFNX-2) |
| OMIM ID |
304400 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked recessive |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
POU3F4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|