Genetic Diseases, Inborn
Disease ID: disease_node_11057
Connections displayed (default: 10).
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| Dbxref | MESH:D030342, NCI:C3101, SNOMEDCT_US_2023_03_01:32895009, UMLS_CUI:C0019247 |
|---|---|
| Subclassof | DOID_4 |
| Data Source | DOID, MESH |
| Mesh Id | D030342 |
| Mesh Label | Genetic Diseases, Inborn |
| Mesh Subclassof | D009358 |
| Doid Label | genetic disease |
| Doid Description | A disease that has_material_basis_in genetic variations in the human genome. |
| Disease Node Id | disease_node_11057 |
| Doid Id | DOID_630 |
| Label | Genetic Diseases, Inborn |
- Incoming r'ship
SUBCLASS_OFto/from Polygenic Disease(ID:disease_node_17150) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Monogenic Disease(ID:disease_node_13650) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Metabolism, Inborn Errors(ID:disease_node_5171) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Disease(ID:disease_node_2554) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Chromosomal Disease(ID:disease_node_17149) (Disease)