Mitochondrial Complex V (Atp Synthase) Deficiency
Disease ID: disease_node_16791
Connections displayed (default: 10).
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| Dbxref | GARD:1459, ORDO:254913, SNOMEDCT_US_2023_03_01:780820008, UMLS_CUI:C4757950 |
|---|---|
| Subclassof | DOID_700 |
| Data Source | DOID |
| Doid Label | mitochondrial complex V (ATP synthase) deficiency |
| Doid Description | A mitochondrial metabolism disease characterized by impaired function of one or more of the proteins making up the mitochondrial proton-transporting ATP synthase complex. |
| Disease Node Id | disease_node_16791 |
| Doid Id | DOID_0111143 |
| Label | Mitochondrial Complex V (Atp Synthase) Deficiency |
- Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex V (Atp Synthase) Deficiency Nuclear Type 2(ID:disease_node_16800) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex V (Atp Synthase) Deficiency Nuclear Type 5(ID:disease_node_16795) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex V (Atp Synthase) Deficiency Nuclear Type 6(ID:disease_node_16792) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex V (Atp Synthase) Deficiency Nuclear Type 7(ID:disease_node_16794) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex V (Atp Synthase) Deficiency Nuclear Type 4(ID:disease_node_16796) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Mitochondrial Diseases(ID:disease_node_10985) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex V (Atp Synthase) Deficiency Nuclear Type 1(ID:disease_node_16801) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex V (Atp Synthase) Deficiency Nuclear Type 3(ID:disease_node_16799) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Mitochondrial Complex V (Atp Synthase) Deficiency Mitochondrial Type 1(ID:disease_node_16793) (Disease)