WormBase Tree Display for DO_term: DOID:0070485
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| DOID:0070485 | Name | mitochondrial complex IV deficiency nuclear type 23 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A cytochrome-c oxidase deficiency disease characterized by infantile onset encephalopathy that has_material_basis_in homozygous mutation in the COX11 gene on chromosome 17q22. | ||||
| Synonym | Exact | MC4DN23 | |||
| Parent | Is_a | DOID:3762 | |||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 620275 | |
| Attribute_of | Gene_by_orthology | WBGene00010437 |
