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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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MIRAGE
Kufor-Rakeb syndrome
Summary
- Synonym
-
- autosomal recessive Parkinson disease 9
- autosomal recessive juvenile onset Parkinson disease 9
- Definition
- An early-onset Parkinson's disease that is characterized by supranuclear gaze palsy, spasticity, and dementia and has_material_basis_in homozygous or compound heterozygous mutation in a lysosomal type 5 ATPase encoding gene on chromosome 1p36.
- Super Class
- autosomal recessive disease early-onset Parkinson's disease
External Links
- Disease Ontology
- DOID:0060556
- Mondo Disease Ontology
- MeSH
- UMLS
- ORDO
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9NQ11 | Polyamine-transporting ATPase 13A2 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9CTG6 | Polyamine-transporting ATPase 13A2 |
