| Preferred Name |
Demyelination |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C117277 |
| ALT_DEFINITION |
Breakdown, or abnormal development, of a nerve fiber myelin sheath. Loss of myelin with relative preservation of the ensheathed axon, characterized by the presence of myelin ovoids and reduced myelin staining. |
| code |
C117277 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C61410 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C120531 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118464 |
| Contributing_Source |
CDISC NICHD MedDRA |
| DEFINITION |
Breakdown, or abnormal development, of a nerve fiber myelin sheath. |
| FULL_SYN |
Dysmyelination |
| Has_NICHD_Parent | |
| label |
Demyelination |
| NICHD_Hierarchy_Term |
Dysmyelination |
| Preferred_Name |
Demyelination |
| prefixIRI |
C117277 |
| prefLabel |
Demyelination |
| Semantic_Type |
Finding |
| UMLS_CUI |
C0011304 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/OMIM/MTHU002306 | Online Mendelian Inheritance in Man | LOOM |