Myopathies, Structural, Congenital
Disease ID: disease_node_10806
Connections displayed (default: 10).
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| Dbxref | GARD:12719, ICD10CM:G71.228, MESH:D020914, ORDO:169189, SNOMEDCT_US_2023_03_01:716696006, UMLS_CUI:C1834558 |
|---|---|
| Subclassof | DOID_0050736, DOID_14717 |
| Data Source | DOID, MESH |
| Synonyms | AD-CNM |
| Mesh Id | D020914 |
| Mesh Label | Myopathies, Structural, Congenital |
| Mesh Subclassof | D009135 |
| Doid Label | autosomal domit centronuclear myopathy |
| Doid Description | A centronuclear myopathy that has_material_basis_in autosomal domit inheritance. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_10806 |
| Doid Id | DOID_0111217 |
| Label | Myopathies, Structural, Congenital |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Centronuclear Myopathy 1(ID:disease_node_18928) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Centronuclear Myopathy 4(ID:disease_node_18927) (Disease)