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
amyotrophic lateral sclerosis type 10
Summary
- Synonym
-
- ALS10
- TARDBP-related frontotemporal lobar degeneration with TDP43 inclusions
- amyotrophic lateral sclerosis 10
- amyotrophic lateral sclerosis 10, with or without frontotemporal dementia
- Definition
- An amyotrophic lateral sclerosis that has_material_basis_in mutation in the TARDBP gene on chromosome 1.
- Super Class
- amyotrophic lateral sclerosis
External Links
- Disease Ontology
- DOID:0060201
- Mondo Disease Ontology
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002145 | Frontotemporal dementia |
| HP:0000716 | Depression |
| HP:0002360 | Sleep abnormality |
| HP:0001257 | Spasticity |
| HP:0000712 | Emotional lability |
| HP:0002017 | Nausea and vomiting |
| HP:0002463 | Language impairment |
| HP:0003487 | Babinski sign |
| HP:0012378 | Fatigue |
| HP:0003324 | Generalized muscle weakness |
