Disease #00017
Official abbreviation |
MC3DN1 |
Name |
Mitochondrial complex III deficiency, nuclear type 1, 124000 (3) |
OMIM ID |
124000 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 2 genes |
BCS1L, UQCRB |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|