Disease #00072
| Official abbreviation |
LHON |
| Name |
LEBER OPTIC ATROPHY, LEBER HEREDITARY OPTIC NEUROPATHY; DOID:705 |
| OMIM ID |
535000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 10 genes |
, MT-ATP6, MT-CO3, MT-CYB, MT-ND1, MT-ND2, MT-ND4, MT-ND4L, MT-ND5, MT-ND6 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|
