Disease #00159
Official abbreviation |
500008 |
Name |
DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL |
OMIM ID |
500008 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 6 genes |
, MT-ND1, MT-RNR1, MT-TH, MT-TI, MT-TS1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|