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congenital myasthenic syndrome 7
Summary
- Synonym
-
- CMS7
- congenital myasthenic syndrome 7 presynaptic
- Definition
- A congenital myasthenic syndrome characterized by autosomal dominant inheritance of presynaptic defects with onset of symptoms in early childhood that has_material_basis_in heterozygous mutation in the SYT2 gene on chromosome 1q32.
- Super Class
- autosomal dominant disease congenital myasthenic syndrome
External Links
- Disease Ontology
- DOID:0110659
- Mondo Disease Ontology
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0004889 | Intermittent episodes of respiratory insufficiency due to muscle weakness |
| HP:0011968 | Feeding difficulties |
| HP:0004661 | Frontalis muscle weakness |
| HP:0010536 | Central sleep apnea |
| HP:0100285 | EMG: impaired neuromuscular transmission |
| HP:0007178 | Motor polyneuropathy |
| HP:0003701 | Proximal muscle weakness |
| HP:0010307 | Stridor |
| HP:0012801 | Narrow jaw |
| HP:0005943 | Respiratory arrest |
