Disease #00021 (DFNX1 (deafness, X-linked, type 1 (DFNX-1)), OMIM:304500)
| Official abbreviation |
DFNX1 |
| Name |
deafness, X-linked, type 1 (DFNX-1) |
| OMIM ID |
304500 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
PRPS1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-07-30 11:15:12 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|