Infantile Histiocytoid Cardiomyopathy
Disease ID: disease_node_16949
Connections displayed (default: 10).
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| Dbxref | GARD:9511, MIM:500000 |
|---|---|
| Subclassof | DOID_0050177, DOID_0060036 |
| Data Source | DOID |
| Doid Label | infantile histiocytoid cardiomyopathy |
| Doid Description | An intrinsic cardiomyopathy characterized by the presence of characteristic pale granular foamy histiocyte-like cells within the myocardium and has_material_basis_in a mutation in the gene encoding mitochondrial cytochrome b. |
| Disease Node Id | disease_node_16949 |
| Doid Id | DOID_0080198 |
| Disease Has Basis In | SO_0000704 |
| Label | Infantile Histiocytoid Cardiomyopathy |
- Outgoing r'ship
SUBCLASS_OFto/from Monogenic Disease(ID:disease_node_13650) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Intrinsic Cardiomyopathy(ID:disease_node_16869) (Disease)