Chromosome 16P12.1 Deletion Syndrome
Disease ID: disease_node_17110
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| Dbxref | MIM:136570 |
|---|---|
| Subclassof | DOID_0060388 |
| Data Source | DOID |
| Doid Label | chromosome 16p12.1 deletion syndrome |
| Doid Description | A chromosomal deletion syndrome that has_material_basis_in a 520 kb deletion on the short (p) arm of the chromosome at a location designated 16p12.1 and is characterized by developmental delay, craniofacial dysmorphology, and congenital heart defects. |
| Disease Node Id | disease_node_17110 |
| Doid Id | DOID_0060399 |
| Label | Chromosome 16P12.1 Deletion Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Deletion Syndrome(ID:disease_node_15239) (Disease)