Search Ontology:
Human Disease
Langerhans-cell histiocytosis
- Term ID
- DOID:2571
- Synonyms
-
- Histiocytosis X
- Langerhan's cell histiocytosis
- Langerhans cell granulomatosis
- Letterer-Siwe disease
- Letterer-Siwe disease involving intra-abdominal lymph nodes
- Letterer-Siwe disease involving intrapelvic lymph nodes
- Letterer-Siwe disease involving intrathoracic lymph nodes
- Letterer-Siwe disease involving lymph nodes of axilla and upper limb
- Letterer-Siwe disease involving lymph nodes of head, face and neck
- Letterer-Siwe disease involving lymph nodes of head, face, and neck
- Letterer-Siwe disease involving lymph nodes of inguinal region and lower limb
- Letterer-Siwe disease involving lymph nodes of multiple sites
- Letterer-Siwe disease involving spleen
- Letterer-Siwe disease of intra-abdominal lymph nodes
- Letterer-Siwe disease of intrapelvic lymph nodes
- Letterer-Siwe disease of intrathoracic lymph nodes
- Letterer-Siwe disease of lymph nodes of axilla and upper limb
- Letterer-Siwe disease of lymph nodes of axilla and/or upper limb
- Letterer-Siwe disease of lymph nodes of head, face and neck
- Letterer-Siwe disease of lymph nodes of head, face and/or neck
- Letterer-Siwe disease of lymph nodes of inguinal region amd/or lower limb
- Letterer-Siwe disease of lymph nodes of inguinal region and lower limb
- Letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb
- Letterer-Siwe disease of lymph nodes of multiple sites
- Letterer-Siwe disease of spleen
- Definition
- A histiocytosis that is characterized by clonal proliferation of Langerhans cells. http://en.wikipedia.org/wiki/Langerhans_cell_histiocytosis
- References
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- ICD10CM:C96.0
- ICD10CM:C96.6
- ICD9CM:202.5
- ICDO:9751/1
- MESH:C538636
- MESH:D006646
- MIM:246400
- MIM:604856
- NCI:C3107
- NCI:C3160
- SNOMEDCT_US_2023_03_01:154583006
- SNOMEDCT_US_2023_03_01:234439008
- UMLS_CUI:C0019621
- UMLS_CUI:C0023381
- Ontology
- Human Disease ( DOID:2571 )
- is a type of
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Genes Involved
Zebrafish Models