Disease #00038 (LS (Leigh syndrome (LS)), OMIM:256000)
| Official abbreviation |
LS |
| Name |
Leigh syndrome (LS) |
| OMIM ID |
256000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 16 genes |
BCS1L, COX10, COX15, FOXRED1, NDUFA10, NDUFA12, NDUFA2, NDUFA9, NDUFAF2, NDUFAF6, NDUFS3, NDUFS4, NDUFS7, NDUFS8, SDHA, SURF1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-08-30 16:26:44 +02:00 (CEST) |
| Date last edited |
N/A |
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