Chromosome 19P13.13 Deletion Syndrome
Disease ID: disease_node_17097
Connections displayed (default: 10).
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| Dbxref | MIM:613638 |
|---|---|
| Subclassof | DOID_0050736, DOID_0060388 |
| Data Source | DOID |
| Doid Label | chromosome 19p13.13 deletion syndrome |
| Doid Description | A chromosomal deletion syndrome that has_material_basis_in a chromosome 19p13.13 deletion and that is characterized by an unusually large head size, tall stature, and intellectual disability that is usually moderate in severity. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17097 |
| Doid Id | DOID_0060426 |
| Label | Chromosome 19P13.13 Deletion Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Chromosomal Deletion Syndrome(ID:disease_node_15239) (Disease)