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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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GALAXY
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MIRAGE
Canavan disease
Summary
- Synonym
-
- ACY2 DEFICIENCY
- AMINOACYLASE 2 DEFICIENCY
- ASP DEFICIENCY
- ASPA DEFICIENCY
- ASPARTOACYLASE DEFICIENCY
- CANAVAN-VAN BOGAERT-BERTRAND DISEASE
- Spongy degeneration of central nervous system
- Definition
- A leukodystrophy characterized by onset in early infancy, atonia of neck muscles, hypotonia, hyperextension of legs and flexion of arms, blindness, severe mental defect, megalocephaly, and death by 18 months on the average that has_material_basis_in homozygous or compound heterozygous mutation in ASPA gene encoding aspartoacylase on chromosome 17p13.
- Super Class
- autosomal recessive disease leukodystrophy
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q3TJA2 | Superoxide dismutase |
