Familial Restrictive Cardiomyopathy 6
Disease ID: disease_node_16874
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:619433 |
|---|---|
| Subclassof | DOID_397, DOID_0050737 |
| Data Source | DOID |
| Synonyms | RCM6, restrictive cardiomyopathy 6 |
| Doid Label | familial restrictive cardiomyopathy 6 |
| Doid Description | A restrictive cardiomyopathy characterized by prenatal onset of severe restrictive cardiomyopathy predomitly involving the right ventricle, resulting in irreversible heart failure and early death that has_material_basis_in compound heterozygous mutation in the KIF20A gene on chromosome 5q31. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16874 |
| Doid Id | DOID_0061025 |
| Label | Familial Restrictive Cardiomyopathy 6 |
- Outgoing r'ship
SUBCLASS_OFto/from Cardiomyopathy, Restrictive(ID:disease_node_1869) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)