Disease #05179 (MTCO1 (deficiency, cytochrome Coxidase subunit I (MTCO-1)), OMIM:516030)
| Official abbreviation |
MTCO1 |
| Name |
deficiency, cytochrome Coxidase subunit I (MTCO-1) |
| OMIM ID |
516030 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
MT-CO1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2016-09-13 15:57:13 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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