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
Gaucher's disease type III
Summary
- Synonym
-
- GD III
- Gaucher Disease, Chronic Neuronopathic Type
- Gaucher Disease, Juvenile And Adult, Cerebral
- Gaucher Disease, Subacute Neuronopathic Type
- Definition
- A Gaucher's disease characterized by later onset and slower progession of neurological deterioration compared to type II that has_material_basis_in homozygous or compound heterozygous mutation in the GBA1 gene on chromosome 1q22.
- Super Class
- Gaucher's disease autosomal recessive disease
External Links
- Disease Ontology
- DOID:0110959
- Mondo Disease Ontology
- ORDO
- OMIM
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P04062 | Lysosomal acid glucosylceramidase | |
| P12821 | Angiotensin-converting enzyme | |
| Q13231 | Chitotriosidase-1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002205 | Recurrent respiratory infections |
| HP:0006530 | Abnormal pulmonary interstitial morphology |
| HP:0001698 | Pericardial effusion |
| HP:0003581 | Adult onset |
| HP:0004934 | Vascular calcification |
| HP:0002167 | Abnormality of speech or vocalization |
| HP:0004322 | Short stature |
| HP:0011463 | Childhood onset |
| HP:0001270 | Motor delay |
| HP:0002313 | Spastic paraparesis |
