Langerhans-cell histiocytosis (DOID:2571)
Alliance: disease page
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
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:C96.6, ICD9CM_2006:202.51, ICD9CM_2006:202.52, ICD9CM_2006:202.53, ICD9CM_2006:202.54, ICD9CM_2006:202.55, ICD9CM_2006:202.56, ICD9CM_2006:202.57, ICD9CM_2006:202.58, ICD9CM:202.5, MESH:C538636, MESH:D006646, NCI:C3107, NCI:C3160, UMLS_CUI:C0019621, UMLS_CUI:C0023381
Definition: A histiocytosis that is characterized by clonal proliferation of Langerhans cells.