Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
congenital myasthenic syndrome 21
Summary
- Synonym
-
- CMS21
- congenital myasthenic syndrome 21, presynaptic
- Definition
- A congenital myasthenic syndrome characterized by autosomal recessive inheritance of hypotonia, apneas, and feeding difficulties that has_material_basis_in homozygous or compound heterozygous mutation in the SLC18A3 gene on chromosome 10q11.
- Super Class
- autosomal recessive disease congenital myasthenic syndrome
External Links
- Disease Ontology
- DOID:0110672
- Mondo Disease Ontology
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000369 | Low-set ears |
| HP:0000565 | Esotropia |
| HP:0000276 | Long face |
| HP:0000639 | Nystagmus |
| HP:0000467 | Neck muscle weakness |
| HP:0000218 | High palate |
| HP:0000508 | Ptosis |
| HP:0000308 | Microretrognathia |
| HP:0000602 | Ophthalmoplegia |
| HP:0000407 | Sensorineural hearing impairment |
