Disease #00018
Official abbreviation |
MC3DN2 |
Name |
Mitochondrial complex III deficiency, nuclear type 2, 615157 (3) |
OMIM ID |
615157 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
TTC19 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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