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congenital myasthenic syndrome 6
Summary
- Synonym
-
- CMS Ia2
- CMS1A2
- CMS6
- CMSEA
- FIM
- FIMG2
- congenital myasthenic syndrome 6, presynaptic
- congenital myasthenic syndrome type Ia2
- congenital presynaptic myasthenic syndrome associated with episodic apnea
- familial infantile myasthenia
- familial infantile myasthenia gravis 2
- Definition
- A congenital myasthenic syndrome characterized by autosomal recessive inheritance of a presynaptic defect resulting in onset of muscle weakeness in infancy or early childhood and a tendency to have sudden apneic episodes that has_material_basis_in homozygous or compound heterozygous mutation in the CHAT gene on chromosome 10q.
- Super Class
- autosomal recessive disease congenital myasthenic syndrome
External Links
- Disease Ontology
- DOID:0110671
- Mondo Disease Ontology
- OMIM
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P28329 | Choline O-acetyltransferase |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0011968 | Feeding difficulties |
| HP:0012801 | Narrow jaw |
| HP:0100285 | EMG: impaired neuromuscular transmission |
| HP:0100295 | Muscle fiber atrophy |
| HP:0003403 | EMG: decremental response of compound muscle action potential to repetitive nerve stimulation |
| HP:0000597 | Ophthalmoparesis |
| HP:0003623 | Neonatal onset |
| HP:0000486 | Strabismus |
| HP:0003397 | Generalized hypotonia due to defect at the neuromuscular junction |
| HP:0003554 | Type 2 muscle fiber atrophy |
