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metachromatic leukodystrophy
Summary
- Synonym
-
- MLD
- Scholz cerebral sclerosis
- arylsulfatase A deficiency
- deficiency of cerebroside-sulfatase
- sulfatide lipoidosis
- Definition
- A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.
- Super Class
- sphingolipidosis
External Links
- Disease Ontology
- DOID:10581
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 410 | ARSA | arylsulfatase A | |
| 411 | ARSB | arylsulfatase B | |
| 412 | STS | steroid sulfatase | |
| 2523 | FUT1 | fucosyltransferase 1 (H blood group) | |
| 2581 | GALC | galactosylceramidase | |
| 2588 | GALNS | galactosamine (N-acetyl)-6-sulfatase | |
| 2629 | GBA1 | glucosylceramidase beta 1 | |
| 2720 | GLB1 | galactosidase beta 1 | |
| 3423 | IDS | iduronate 2-sulfatase | |
| 5660 | PSAP | prosaposin |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P34059 | N-acetylgalactosamine-6-sulfatase | |
| P54803 | Galactocerebrosidase | |
| Q8NBK3 | Formylglycine-generating enzyme | |
| Q96EG1 | Arylsulfatase G |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0011096 | Peripheral demyelination |
| HP:0001263 | Global developmental delay |
| HP:0001271 | Polyneuropathy |
| HP:0001285 | Spastic tetraparesis |
| HP:0002015 | Dysphagia |
| HP:0002333 | Motor deterioration |
| HP:0002505 | Loss of ambulation |
| HP:0002518 | Abnormal periventricular white matter morphology |
| HP:0007305 | CNS demyelination |
| HP:0009830 | Peripheral neuropathy |
