Disease #00475 (albinism, ocular, with sensorineural deafness (Waardenburg syndrome, (WS-2OA)), OMIM:103470)
| Official abbreviation |
- |
| Name |
albinism, ocular, with sensorineural deafness (Waardenburg syndrome, (WS-2OA)) |
| OMIM ID |
103470 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
MITF, TYR |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-07-24 21:39:44 +02:00 (CEST) |
| Date last edited |
N/A |
|
|
