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Langerhans-cell histiocytosis (DOID:2571)
Synonyms: Histiocytosis X; Langerhan's cell histiocytosis (disorder); 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 intra-abdominal lymph nodes (disorder); Letterer-Siwe disease of intrapelvic lymph nodes; Letterer-Siwe disease of intrapelvic lymph nodes (disorder); Letterer-Siwe disease of intrathoracic lymph nodes; Letterer-Siwe disease of intrathoracic lymph nodes (disorder); Letterer-Siwe disease of lymph nodes of axilla and upper limb (disorder); Letterer-Siwe disease of lymph nodes of axilla and/or upper limb; Letterer-Siwe disease of lymph nodes of axilla and/or upper limb (disorder); Letterer-Siwe disease of lymph nodes of head, face and neck (disorder); Letterer-Siwe disease of lymph nodes of head, face and/or neck (disorder); 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 (disorder); Letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb (disorder); Letterer-Siwe disease of lymph nodes of multiple sites; Letterer-Siwe disease of lymph nodes of multiple sites (disorder); Letterer-Siwe disease of spleen; Letterer-Siwe disease of spleen (disorder)
Alt IDs: OMIM:246400, OMIM:604856, DOID:10617, DOID:10618, DOID:10620, DOID:10623, DOID:10624, DOID:10625, DOID:2553, DOID:2554, DOID:9582, ICD10CM:C96.0, ICD10CM:C96.5, ICD10CM:C96.6, ICD9CM:202.5, MESH:C538636, MESH:D006646, NCI:C3107, NCI:C3160, NCI:C6920, UMLS_CUI:C0019621, UMLS_CUI:C0023381
Definition: A histiocytosis that is characterized by clonal proliferation of Langerhans cells.


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last database update
07/11/2017
MGI 6.10
The Jackson Laboratory