Showing entry for Metachromatic Leukodystrophy due to Saposin B Deficiency
| General Disease Information | |
|---|---|
| BXGD Id | BXGD005872 |
| Disease Name | Metachromatic Leukodystrophy due to Saposin B Deficiency |
| Disease CUI Id | C0268262 |
| MeSH Codes | C16 C18 C10 |
| Disease Class Name | Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| Semantic Type | Disease or Syndrome |
| Human Phenotype Ontology Id | |
| Human Phenotype Ontology Term | |
| Disease Ontology Id | DOID:0014667 DOID:630 |
| Disease Ontology Class Name | disease of metabolism; genetic disease |
| Disorder Network | disorder-protein-compound-food associations
|