Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (disorder)
| Code | 1172899000 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | primitive |
| Effective time | 20210930 |
4881200417q partial trisomy syndrome
disorder
11164009Autosomal dominant hereditary disorder
disorder
276654001Congenital malformation
disorder
363070008Developmental hereditary disorder
disorder
1362108000Genetic intellectual disability
disorder
224958001Global developmental delay
disorder
398100001Hereditary motor and sensory neuropathy
disorder
1137472008Neurodevelopmental delay
disorder
None (leaf concept).