WormBase Tree Display for DO_term: DOID:0080359
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| DOID:0080359 | Name | mitochondrial complex IV deficiency nuclear type 9 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A COX deficiency, infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COA5 gene on chromosome 2q11. | ||||
| Synonym | Exact | MC4DN9 | |||
| fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 3 | |||||
| Parent | Is_a | DOID:0050713 | |||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 616500 | |
| Attribute_of | Gene_by_orthology | WBGene00012483 |
