Disease #00015
Official abbreviation |
LS |
Name |
Leigh syndrome due to mitochondrial complex 1 deficiency, 256000 (3) |
OMIM ID |
256000 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
LIPT1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
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