Chromosome Xp11.3 microdeletion syndrome (disorder)
| Code | 719808002 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | primitive |
| Effective time | 20170131 |
111312006Anomaly of chromosome X
disorder
276654001Congenital malformation
disorder
363070008Developmental hereditary disorder
disorder
1362108000Genetic intellectual disability
disorder
1162976004X-linked recessive hereditary disease
disorder
232054005X-linked retinitis pigmentosa
disorder
None (leaf concept).