WormBase Tree Display for DO_term: DOID:0112097
expand all nodes | collapse all nodes | view schema
DOID:0112097 | Name | nuclear type mitochondrial complex I deficiency 33 | |||
---|---|---|---|---|---|
Status | Valid | ||||
Definition | A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA6 gene on chromosome 22q13.2. | ||||
Synonym | Exact | MC1DN33 | |||
Parent | Is_a | DOID:0050737 | |||
DOID:0112065 | |||||
DB_info | Database | OMIM | disease | 618253 | |
Attribute_of | Gene_by_orthology | WBGene00013308 |