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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
lysosomal acid lipase deficiency
Summary
- Synonym
-
- LAL deficiency
- LAL-D
- Definition
- A lipid storage disease characterized by dyslipidemia and accumulation of cholesteryl esters and triglycerides within various organs that has_material_basis_in homozygous or compound heterozygous mutation in the LIPA gene on chromosome 10q23.31.
- Super Class
- autosomal recessive disease lipid storage disease
External Links
- Disease Ontology
- DOID:0080217
- Mondo Disease Ontology
- UMLS
- ORDO
- GARD
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P38571 | Lysosomal acid lipase/cholesteryl ester hydrolase |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002240 | Hepatomegaly |
| HP:0002570 | Steatorrhea |
| HP:0003270 | Abdominal distention |
| HP:0004326 | Cachexia |
| HP:0004333 | Bone-marrow foam cells |
| HP:0004395 | Malnutrition |
| HP:0010512 | Adrenal calcification |
| HP:0000952 | Jaundice |
| HP:0000989 | Pruritus |
| HP:0001394 | Cirrhosis |
