|
| General Information | |||
|---|---|---|---|
| Term | neurosarcoidosis | ID (Ontology) | DOID:13403 (Human Disease) |
| Definition | A sarcoidosis that is characterized by involvement of the nervous symptom with cranial nerve palsy, diffuse meningeal disease, acute polyneuropathy, myelitis, or hypothalamic pituitary axis malformation, develops_from a type IV hypersensitivity reaction with noncaseating granulomas involving the nervous system. | ||
| Also Known As | "cerebral sarcoidosis" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
hypersensitivity reaction type IV disease |__sarcoidosis |__neurosarcoidosis |__sarcoid meningitis |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | sarcoidosis | ||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
|
NCI:C35441 SNOMEDCT_US_2023_03_01:111936002 UMLS_CUI:C0398676 |
|||