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congenital myasthenic syndrome 3B
Summary
- Synonym
-
- CMS3B
- congenital myasthenic syndrome 3B, fast-channel
- Definition
- A congenital myasthenic syndrome characterized by autosomal recessive inheritance of postsynaptic neuromuscular junction defects resulting in rapid decay in endplate current and a failure to reach the threshold for depolarization and early onset progressive muscular weakness that has_material_basis_in homozygous or compound heterozygous mutation in the CHRND gene on chromosome 2q37.
- Super Class
- autosomal recessive disease congenital myasthenic syndrome
External Links
- Disease Ontology
- DOID:0110665
- Mondo Disease Ontology
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 42918 | nAChRalpha1 | nicotinic Acetylcholine Receptor alpha1 | |
| 42919 | nAChRalpha2 | nicotinic Acetylcholine Receptor alpha2 | |
| 42920 | nAChRbeta2 | nicotinic Acetylcholine Receptor beta2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000961 | Cyanosis |
| HP:0002792 | Reduced vital capacity |
| HP:0000218 | High palate |
| HP:0003202 | Skeletal muscle atrophy |
| HP:0001446 | Abnormality of the musculature of the upper limbs |
| HP:0003443 | Decreased size of nerve terminals |
| HP:0000651 | Diplopia |
| HP:0002650 | Scoliosis |
| HP:0003484 | Upper limb muscle weakness |
| HP:0001315 | Reduced tendon reflexes |
