Dilated Cardiomyopathy 2E
Disease ID: disease_node_16921
Connections displayed (default: 10).
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| Dbxref | MIM:619492 |
|---|---|
| Subclassof | DOID_12930, DOID_0050737 |
| Data Source | DOID |
| Doid Label | dilated cardiomyopathy 2E |
| Doid Description | A dilated cardiomyopathy that is characterized by neonatal or early childhood onset of dilated cardiomyopathy, with rapid progression to cardiac failure and death unless patients undergo cardiac transplantation and that has_material_basis_in homozygous or compound heterozygous mutation in the JPH2 gene on chromosome 20q13. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16921 |
| Doid Id | DOID_0081161 |
| Label | Dilated Cardiomyopathy 2E |
- Outgoing r'ship
SUBCLASS_OFto/from Cardiomyopathy, Dilated(ID:disease_node_1864) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)