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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:0000651 | Diplopia |
| HP:0000768 | Pectus carinatum |
| HP:0000961 | Cyanosis |
| HP:0001249 | Intellectual disability |
| HP:0001250 | Seizure |
| HP:0001251 | Ataxia |
| HP:0001252 | Hypotonia |
| HP:0001265 | Hyporeflexia |
| HP:0001270 | Motor delay |
| HP:0001283 | Bulbar palsy |
