Ehlers-Danlos Syndrome Cardiac Valvular Type
Disease ID: disease_node_18767
Connections displayed (default: 10).
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| Dbxref | MIM:225320 |
|---|---|
| Subclassof | DOID_0050737, DOID_13359 |
| Data Source | DOID |
| Doid Label | Ehlers-Danlos syndrome cardiac valvular type |
| Doid Description | An Ehlers-Danlos syndrome that is characterized by severe problems with heart valves and that has_material_basis_in homozygous or compound heterozygous mutation in the COL1A2 gene on chromosome 7q21. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_18767 |
| Doid Id | DOID_0080730 |
| Label | Ehlers-Danlos Syndrome Cardiac Valvular Type |
- Outgoing r'ship
SUBCLASS_OFto/from Ehlers-Danlos Syndrome(ID:disease_node_2744) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)