Nuclear Type Mitochondrial Complex I Deficiency 35
Disease ID: disease_node_17013
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| Dbxref | MIM:619003 |
|---|---|
| Subclassof | DOID_0050737, DOID_0060536 |
| Data Source | DOID |
| Synonyms | MC1DN35 |
| Doid Label | nuclear type mitochondrial complex I deficiency 35 |
| Doid Description | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFB10 gene on chromosome 16p13.3. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17013 |
| Doid Id | DOID_0112139 |
| Label | Nuclear Type Mitochondrial Complex I Deficiency 35 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)