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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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MIRAGE
amyotrophic lateral sclerosis type 6
Summary
- Synonym
-
- ALS6
- amyotrophic lateral sclerosis 6, with or without frontotemporal dementia
- autosomal recessive amyotrophic lateral sclerosis 6
- Definition
- An amyotrophic lateral sclerosis that has_material_basis_in mutation in the FUS gene on chromosome 16.
- Super Class
- amyotrophic lateral sclerosis
External Links
- Disease Ontology
- DOID:0060198
- Mondo Disease Ontology
- GARD
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P35637 | RNA-binding protein FUS |
| UniProt ID | Protein Name | Source |
|---|---|---|
| P56959 | RNA-binding protein FUS |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0100543 | Cognitive impairment |
| HP:0008955 | Progressive distal muscular atrophy |
| HP:0012531 | Pain |
| HP:0009067 | Progressive spinal muscular atrophy |
| HP:0007373 | Motor neuron atrophy |
| HP:0012378 | Fatigue |
| HP:0008322 | Abnormal mitochondrial morphology |
| HP:0002283 | Global brain atrophy |
| HP:0000605 | Supranuclear gaze palsy |
| HP:0002314 | Degeneration of the lateral corticospinal tracts |
