Group of disorders which feature accumulations of active HISTIOCYTES and LYMPHOCYTES, but where the histiocytes are not LANGERHANS CELLS. The group includes HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; SINUS HISTIOCYTOSIS; xanthogranuloma; reticulohistiocytoma; juvenile XANTHOGRANULOMA; xanthoma disseminatum; as well as the lipid storage diseases (SEA-BLUE HISTIOCYTE SYNDROME; and NIEMANN-PICK DISEASES). [ MESH:D015616 ]
Synonyms: non-Langerhans-cell histiocytosis
Term information
- ICD9:288.4 (MONDO:i2s)
- DOID:4330 (MONDO:equivalentTo)
- Orphanet:157987 (MONDO:equivalentTo)
- UMLS:C0019624 (MONDO:equivalentTo)
- SCTID:127069007 (MONDO:equivalentTo)
- MESH:D015616 (Orphanet:157987/e)
- GARD:8231 (MONDO:GARD)
- MEDGEN:9265 (MONDO:equivalentTo)
gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders
http://identifiers.org/medgen/9265
http://purl.obolibrary.org/obo/DOID_4330
http://identifiers.org/snomedct/127069007
http://www.orpha.net/ORDO/Orphanet_157987
http://linkedlifedata.com/resource/umls/id/C0019624
http://identifiers.org/mesh/D015616