1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0060401 | chromosome 16q22 deletion syndrome | A chromosomal deletion syndrome that has_material_basis_in an interstitial 16q22 deletion that is characterized by a failure to thrive in infancy, poor growth, delayed psychomotor development, hypotonia, and dysmorphic features, including large anterior fontanel, high forehead, diastasis of the cranial sutures, broad nasal bridge, hypertelorism, low-set abnormal ears, and short neck. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0060388 | chromosomal deletion syndrome | A chromosomal disease that has_material_basis_in partial deletion of chromosomes. |
