Disease #00149
| Official abbreviation |
LDYT |
| Name |
LEBER OPTIC ATROPHY AND DYSTONIA, alt: LEBER HEREDITARY OPTIC NEUROPATHY WITH DYSTONIA; LDYT;; DYSTONIA, FAMILIAL, WITH VISUAL FAILURE AND STRIATAL LUCENCIES;; MARSDEN SYNDROME |
| OMIM ID |
500001 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 4 genes |
MT-ND1, MT-ND3, MT-ND4, MT-ND6 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|
