Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome (disorder)
| Code | 1237514002 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | primitive |
| Effective time | 20220930 |
1899006Autosomal hereditary disorder
disorder
85102008Cerebellar ataxia
disorder
248290002Developmental delay
disorder
363070008Developmental hereditary disorder
disorder
763597000Hereditary ataxia
disorder
37650008Hereditary cerebellar degeneration
disorder
363212003Hereditary disorder of musculoskeletal system
disorder
128190004Inherited metabolic disorder of nervous system
disorder
16851005Mitochondrial myopathy
disorder
None (leaf concept).