| Metadata | |
|---|---|
| ID | DOID:0080116 |
| Name | mitochondrial complex III deficiency nuclear type 7 |
| Definition | A mitochondrial complex III deficiency that has_material_basis_in homozygous mutation in the UQCC2 gene on chromosome 6p21. http://omim.org/entry/615824?search=615824&highlight=615824 |
| Xrefs | |
| Parent Relationships | |
| Subclass Logical Relationships |
disease has basis in some structural_variant |