Cox Deficiency, Benign Infantile Mitochondrial Myopathy
Disease ID: disease_node_16766
Connections displayed (default: 10).
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| Dbxref | GARD:48, ORDO:254905, UMLS_CUI:C5779825 |
|---|---|
| Subclassof | DOID_3762 |
| Data Source | DOID |
| Synonyms | Isolated cytochrome C oxidase deficiency |
| Doid Label | COX deficiency, benign infantile mitochondrial myopathy |
| Doid Description | A cytochrome-c oxidase deficiency disease characterized by localization to tissues of the skeletal muscles. |
| Disease Node Id | disease_node_16766 |
| Doid Id | DOID_0081377 |
| Label | Cox Deficiency, Benign Infantile Mitochondrial Myopathy |
- Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 3(ID:disease_node_16777) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 19(ID:disease_node_16782) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 1(ID:disease_node_16778) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 12(ID:disease_node_16771) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 4(ID:disease_node_16776) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 15(ID:disease_node_16769) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 18(ID:disease_node_16783) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 7(ID:disease_node_16775) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 22(ID:disease_node_16779) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 10(ID:disease_node_16773) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 21(ID:disease_node_16780) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 20(ID:disease_node_16781) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 14(ID:disease_node_16770) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 11(ID:disease_node_16772) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 17(ID:disease_node_16767) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 8(ID:disease_node_16774) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex Iv Deficiency Nuclear Type 16(ID:disease_node_16768) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Cytochrome-C Oxidase Deficiency(ID:disease_node_11065) (Disease)