Combined oxidative phosphorylation defect type 23 (disorder)
| Code | 1173036000 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | primitive |
| Effective time | 20210930 |
85995004Autosomal recessive hereditary disorder
disorder
363005004Cardiovascular system hereditary disorder
disorder
363070008Developmental hereditary disorder
disorder
237986005Disorder of mitochondrial respiratory chain complexes
disorder
1362108000Genetic intellectual disability
disorder
128190004Inherited metabolic disorder of nervous system
disorder
472315005Mitochondrial cardiomyopathy
disorder
240096000Mitochondrial cytopathy
disorder
None (leaf concept).