loading...| Preferred Name |
leukodystrophy disease specific cell type |
| Definitions |
Leukodystrophy is a term for a group of white matter diseases, some familial, characterized by progressive cerebral deterioration usually in early life, and pathologically by primary absence or degeneration of the myelin of the central and peripheral nervous systems with glial reaction; probably related to a defect in lipid metabolism. |
| ID |
http://purl.obolibrary.org/obo/BTO_0005830 |
| created_by |
Marion, contact@brenda-enzymes.org |
| creation_date |
2016-04-18T09:29:37Z |
| definition |
Leukodystrophy is a term for a group of white matter diseases, some familial, characterized by progressive cerebral deterioration usually in early life, and pathologically by primary absence or degeneration of the myelin of the central and peripheral nervous systems with glial reaction; probably related to a defect in lipid metabolism. |
| disease causes dysfunction of | |
| has_obo_namespace |
BrendaTissueOBO |
| id |
BTO:0005830 |
| label |
leukodystrophy disease specific cell type |
| notation |
BTO:0005830 |
| prefLabel |
leukodystrophy disease specific cell type |
| treeView | |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| There are currently no mappings for this class. | |||