Nuclear Type Mitochondrial Complex I Deficiency 17
Disease ID: disease_node_17001
Connections displayed (default: 10).
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| Dbxref | MIM:618239 |
|---|---|
| Subclassof | DOID_0112065, DOID_0050737 |
| Data Source | DOID |
| Synonyms | MC1DN17 |
| Doid Label | nuclear type mitochondrial complex I deficiency 17 |
| Doid Description | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF6 gene on chromosome 8q22.1. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17001 |
| Doid Id | DOID_0112078 |
| Label | Nuclear Type Mitochondrial Complex I Deficiency 17 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Nuclear Type Mitochondrial Complex I Deficiency(ID:disease_node_16979) (Disease)