Disease #02273 (deafness, nonsyndromic sensorineural, mitochondrial, OMIM:500008)
| Official abbreviation |
- |
| Name |
deafness, nonsyndromic sensorineural, mitochondrial |
| OMIM ID |
500008 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
22 |
| Phenotype entries for this disease |
22 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2015-12-08 23:51:33 +01:00 (CET) |
Individuals
|