2p13.2 microdeletion syndrome (disorder)
| Code | 770756008 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | primitive |
| Effective time | 20190131 |
11164009Autosomal dominant hereditary disorder
disorder
726368009Deletion of part of short arm of chromosome 2
disorder
363070008Developmental hereditary disorder
disorder
1362108000Genetic intellectual disability
disorder
65094009Multiple malformation syndrome with facial defects as major feature
disorder
None (leaf concept).