Disease #00020
Official abbreviation |
MC3DN4 |
Name |
Mitochondrial complex III deficiency, nuclear type 4, 615159 (3) |
OMIM ID |
615159 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
UQCRQ |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|