Becker Disease
Disease ID: disease_node_15792
Connections displayed (default: 10).
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| Dbxref | MIM:255300, MIM:255700 |
|---|---|
| Subclassof | DOID_0050737, DOID_2106 |
| Data Source | DOID |
| Doid Label | Becker disease |
| Doid Description | A myotonia congenita that is characterized by muscle stiffness and an inability of the muscle to relax after voluntary contraction and that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding skeletal muscle chloride channel-1 (CLCN1) on chromosome 7q34. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15792 |
| Doid Id | DOID_0081335 |
| Label | Becker Disease |
- Outgoing r'ship
SUBCLASS_OFto/from Myotonia Congenita(ID:disease_node_5387) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)