| General Information | |||
|---|---|---|---|
| Term | non-Langerhans-cell histiocytosis | ID (Ontology) | DOID:4330 (Human Disease) |
| Definition | A histiocytosis that is characterized by the accumulation of histiocytes that do not meet the phenotypic criteria for the diagnosis of Langerhans cells. | ||
| 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
|
|||
|
||||||
lymphatic system disease |__histiocytosis |__non-Langerhans-cell histiocytosis |__adult xanthogranuloma |__Erdheim-Chester disease |__juvenile xanthogranuloma |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | histiocytosis | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
GARD:8231 MESH:D015616 SNOMEDCT_US_2023_03_01:127069007 UMLS_CUI:C0019624 |
|||