Disease #00037 (MC3DN-1 (mitochondrial complex III deficiency, nuclear, type 1 (MC3DN-1)]), OMIM:124000)
| Official abbreviation |
MC3DN-1 |
| Name |
mitochondrial complex III deficiency, nuclear, type 1 (MC3DN-1)] |
| OMIM ID |
124000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
BCS1L, UQCRC2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2012-08-30 16:25:23 +02:00 (CEST) |
| Date last edited |
N/A |
|
