Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
nemaline myopathy 2
Summary
- Synonym
-
- NEM2
- congenital myopathy 2
- nemaline myopathy 2, autosomal recessive
- Definition
- A nemaline myopathy that has_material_basis_in homozygous or compound heterozygous mutation in the NEB gene on chromosome 2q23.
- Super Class
- autosomal recessive disease nemaline myopathy
External Links
- Disease Ontology
- DOID:0110928
- Mondo Disease Ontology
- MeSH
- OMIM
- MGI genotype (from TogoID)
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002705 | High, narrow palate |
| HP:0003324 | Generalized muscle weakness |
| HP:0003458 | EMG: myopathic abnormalities |
| HP:0000218 | High palate |
| HP:0000275 | Narrow face |
| HP:0000347 | Micrognathia |
| HP:0000470 | Short neck |
| HP:0000508 | Ptosis |
| HP:0000767 | Pectus excavatum |
| HP:0000774 | Narrow chest |
