Autosomal Domit Hyaline Body Myopathy
Disease ID: disease_node_18941
Connections displayed (default: 10).
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| Dbxref | MIM:608358 |
|---|---|
| Subclassof | DOID_0050736, DOID_0111267 |
| Data Source | DOID |
| Synonyms | MSMA, Myopathy, myosin storage, autosomal dominant, congenital myopathy 7A, myopathy with lysis of type I myofibrils |
| Doid Label | autosomal domit hyaline body myopathy |
| Doid Description | A hyaline body myopathy that has_material_basis_in heterozygous mutation in MYH7 on 14q11.2. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_18941 |
| Doid Id | DOID_0111269 |
| Label | Autosomal Domit Hyaline Body Myopathy |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hyaline Body Myopathy(ID:disease_node_18940) (Disease)