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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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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
biotin-responsive basal ganglia disease
Summary
- Definition
- A basal ganglia disease that is characterized by recurrent subacute encephalopathy, has_symptom confusion, has_symptom seizure, has_symptom ataxia, has_symptom dystonia, has_symptom supranuclear facial palsy, has_symptom external ophthalmoplegia, and has_symptom dysphagia.
- Super Class
- basal ganglia disease
External Links
- Disease Ontology
- DOID:0050659
- Mondo Disease Ontology
- MeSH
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9BZV2 | Thiamine transporter 2 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q99PL8 | Thiamine transporter 2 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q22931 | Folate-like transporter 3 |
