Chromosome 16Q22 Deletion Syndrome
Disease ID: disease_node_17108
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| Dbxref | MIM:614541 |
|---|---|
| Subclassof | DOID_0060388 |
| Data Source | DOID |
| Doid Label | chromosome 16q22 deletion syndrome |
| Doid Description | 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. |
| Disease Node Id | disease_node_17108 |
| Doid Id | DOID_0060401 |
| Label | Chromosome 16Q22 Deletion Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Deletion Syndrome(ID:disease_node_15239) (Disease)