Nuclear Type Mitochondrial Complex I Deficiency 12
Disease ID: disease_node_16980
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:301020 |
|---|---|
| Subclassof | DOID_0080012, DOID_0112065 |
| Data Source | DOID |
| Synonyms | MC1DN12 |
| Doid Label | nuclear type mitochondrial complex I deficiency 12 |
| Doid Description | A nuclear type mitochondrial complex I deficiency that has_material_basis_in hemizygous mutation in the NDUFA1 gene on chromosome Xq24. |
| Has Material Basis In | GENO_0000149 |
| Disease Node Id | disease_node_16980 |
| Doid Id | DOID_0112099 |
| Label | Nuclear Type Mitochondrial Complex I Deficiency 12 |
- Outgoing r'ship
SUBCLASS_OFto/from Nuclear Type Mitochondrial Complex I Deficiency(ID:disease_node_16979) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from X-Linked Recessive Disease(ID:disease_node_13254) (Disease)