Mitochondrial Complex Iv Deficiency Nuclear Type 7
Disease ID: disease_node_16775
Connections displayed (default: 10).
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| Dbxref | MIM:619051, UMLS_CUI:C5436685 |
|---|---|
| Subclassof | DOID_0050737, DOID_0081377 |
| Data Source | DOID |
| Synonyms | MC4DN7 |
| Doid Label | mitochondrial complex IV deficiency nuclear type 7 |
| Doid Description | A COX deficiency, benign infantile mitochondrial myopathy that has_material_basis_in homozygous mutation in the COX6B1 gene on chromosome 19q13.12. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16775 |
| Doid Id | DOID_0070494 |
| Label | Mitochondrial Complex Iv Deficiency Nuclear Type 7 |
- Outgoing r'ship
SUBCLASS_OFto/from Cox Deficiency, Benign Infantile Mitochondrial Myopathy(ID:disease_node_16766) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)