Dilated Cardiomyopathy 2D
Disease ID: disease_node_16922
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:619371 |
|---|---|
| Subclassof | DOID_12930, DOID_0050737 |
| Data Source | DOID |
| Doid Label | dilated cardiomyopathy 2D |
| Doid Description | A dilated cardiomyopathy that is characterized by neonatal onset of severe cardiomyopathy, with rapid progression to cardiac decompensation and death unless the patient undergoes heart transplantation and that has_material_basis_in homozygous or compound heterozygous mutation in the RPL3L gene on chromosome 16p13. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16922 |
| Doid Id | DOID_0081160 |
| Label | Dilated Cardiomyopathy 2D |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Cardiomyopathy, Dilated(ID:disease_node_1864) (Disease)