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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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glycoproteinosis
Summary
- Synonym
-
- Mucolipidosis type I
- sialidosis
- Definition
- A mucolipidosis that is characterized by a deficiency of the enzyme alpha-N -acetyl neuraminidase (sialidase).
- Super Class
- mucolipidosis
External Links
- Disease Ontology
- DOID:3343
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 353 | APRT | adenine phosphoribosyltransferase | |
| 811 | CALR | calreticulin | |
| 1118 | CHIT1 | chitinase 1 | |
| 1589 | CYP21A2 | cytochrome P450 family 21 subfamily A member 2 | |
| 1717 | DHCR7 | 7-dehydrocholesterol reductase | |
| 1798 | DPAGT1 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | |
| 2519 | FUCA2 | alpha-L-fucosidase 2 | |
| 2720 | GLB1 | galactosidase beta 1 | |
| 2990 | GUSB | glucuronidase beta | |
| 3073 | HEXA | hexosaminidase subunit alpha |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0012061 | Urinary excretion of sialylated oligosaccharides |
| HP:0100022 | Abnormality of movement |
| HP:0100790 | Hernia |
| HP:0001789 | Hydrops fetalis |
| HP:0001347 | Hyperreflexia |
| HP:0004333 | Bone-marrow foam cells |
| HP:0001290 | Generalized hypotonia |
| HP:0001640 | Cardiomegaly |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000093 | Proteinuria |
