Langerhans cell histiocytosis
http://purl.obolibrary.org/obo/MONDO_0018310
Langerhans cell histiocytosis (LCH) is a systemic disease associated with the proliferation and accumulation (usually in granulomas) of Langerhans cells in various tissues. [ Orphanet:389 ]
Term info
- ONCOTREE:LCH (MONDO:equivalentTo)
- ICDO:9751/3 (NCIT:C3107)
- ICDO:9752/1 (NCIT:C3107)
- GARD:0006858 (MONDO:equivalentTo)
- ICDO:9754/3 (NCIT:C3107)
- UMLS:C0432553 (MONDO:equivalentTo)
- UMLS:C0432549 (MONDO:equivalentTo)
- UMLS:C0432554 (MONDO:equivalentTo)
- ICD9:202.5 (DOID:2571)
- UMLS:C0432548 (MONDO:equivalentTo)
- ICDO:9751/1 (NCIT:C3107)
- ICD9:277.89 (MONDO:relatedTo)
- NCIT:C3107 (MONDO:equivalentTo)
- SCTID:65399007 (MONDO:equivalentTo)
- UMLS:C0432550 (MONDO:equivalentTo)
- EFO:1000318 (MONDO:equivalentTo)
- OMIM:604856 (Orphanet:389/e)
- UMLS:C0019621 (Orphanet:389/e)
- ICDO:9753/1 (NCIT:C3107)
- Orphanet:389 (OMIM:604856)
- UMLS:C0432551 (MONDO:equivalentTo)
- UMLS:C0432552 (MONDO:equivalentTo)
- MedDRA:10069698 (Orphanet:389/e)
- UMLS:C0432547 (MONDO:equivalentTo)
- DOID:2571 (MONDO:equivalentTo)
disease_grouping, ordo_group_of_disorders
http://identifiers.org/meddra/10069698
We follow NCIT in classifying this as a neoplasm but this may be revisited
Langerhans cell histiocytosis (LCH) is a systemic disease associated with the proliferation and accumulation (usually in granulomas) of Langerhans cells in various tissues.
http://identifiers.org/snomedct/65399007, https://omim.org/entry/604856, http://purl.obolibrary.org/obo/DOID_2571, http://linkedlifedata.com/resource/umls/id/C0019621, http://linkedlifedata.com/resource/umls/id/C0432553, http://linkedlifedata.com/resource/umls/id/C0432552, http://purl.obolibrary.org/obo/Orphanet_389, http://linkedlifedata.com/resource/umls/id/C0432551, http://linkedlifedata.com/resource/umls/id/C0432550, http://linkedlifedata.com/resource/umls/id/C0432549, http://purl.obolibrary.org/obo/NCIT_C3107, http://linkedlifedata.com/resource/umls/id/C0432548, http://linkedlifedata.com/resource/umls/id/C0432547, http://linkedlifedata.com/resource/umls/id/C0432554
http://purl.obolibrary.org/obo/MONDO_0002332
letterer-Siwe disease of spleen, letterer-Siwe disease of lymph nodes of head, face and/or neck, letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb, letterer-Siwe disease of intrathoracic lymph nodes, letterer-Siwe disease of lymph nodes of inguinal region and lower limb, letterer-Siwe disease involving lymph nodes of inguinal region and lower limb, letterer-Siwe disease involving lymph nodes of multiple sites, Langerhan's cell histiocytosis, letterer-Siwe disease of intra-abdominal lymph nodes, letterer-Siwe disease involving intra-abdominal lymph nodes, Langerhans cell granulomatosis, letterer-Siwe disease involving spleen, letterer-Siwe disease involving lymph nodes of axilla and upper limb, letterer-Siwe disease of lymph nodes of axilla and upper limb, Langerhans cell histiocytosis, letterer-Siwe disease of intrapelvic lymph nodes, letterer-Siwe disease of lymph nodes of head, face and neck, letterer-Siwe disease involving intrathoracic lymph nodes, letterer-Siwe disease of lymph nodes of axilla and/or upper limb, letterer-Siwe disease of lymph nodes of multiple sites, LCH, letterer-Siwe disease involving lymph nodes of head, face and neck, letterer-Siwe disease of lymph nodes of inguinal region amd/or lower limb, Langerhans cell histiocytosis, Not otherwise specified, letterer-Siwe disease involving lymph nodes of head, face, and neck, Langerhans cell histiocytosis, NOS, letterer-Siwe disease involving intrapelvic lymph nodes, histiocytosis X
Lch, Langerhans-cell histiocytosis
MONDO:0018310