WormBase Tree Display for DO_term: DOID:0112086
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| DOID:0112086 | Name | nuclear type mitochondrial complex I deficiency 26 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA9 gene on chromosome 12p13.32. | ||||
| Synonym | Exact | MC1DN26 | |||
| Parent | Is_a | DOID:0050737 | |||
| DOID:0112065 | |||||
| DB_info | Database | OMIM | disease | 618247 | |
| Attribute_of | Gene_by_orthology | WBGene00021800 |
