Chromosomal Disease
Disease ID: disease_node_17149
Connections displayed (default: 10).
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| Subclassof | DOID_630 |
|---|---|
| Data Source | DOID |
| Doid Label | chromosomal disease |
| Doid Description | A genetic disease that has_material_basis_in extra, missing, or re-arranged chromosomes. |
| Disease Node Id | disease_node_17149 |
| Doid Id | DOID_0080014 |
| Label | Chromosomal Disease |
- Incoming r'ship
SUBCLASS_OFto/from Trisomy 13 Syndrome(ID:disease_node_255) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Ring Chromosomes(ID:disease_node_6698) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Prader-Willi Syndrome(ID:disease_node_6283) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Genetic Diseases, Inborn(ID:disease_node_11057) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosomal Deletion Syndrome(ID:disease_node_15239) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosomal Duplication Syndrome(ID:disease_node_13621) (Disease)