WormBase Tree Display for DO_term: DOID:0112069
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DOID:0112069 | Name | nuclear type mitochondrial complex I deficiency 22 | |||
---|---|---|---|---|---|
Status | Valid | ||||
Definition | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA10 gene on chromosome 2q37.3. | ||||
Synonym | Exact | MC1DN22 | |||
Parent | Is_a | DOID:0050737 | |||
DOID:0112065 | |||||
DB_info | Database | OMIM | disease | 618243 | |
Attribute_of | Gene_by_orthology | WBGene00019401 |