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[X] non-Langerhans cell histiocytosis

Go to external page http://purl.obolibrary.org/obo/MONDO_0015531

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

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:157987 (MONDO:equivalentTo)
  • ICD9:288.4 (MONDO:i2s)
  • MESH:D015616 (Orphanet:157987/e)
  • SCTID:127069007 (MONDO:equivalentTo)
  • GARD:8231 (MONDO:GARD)
  • MEDGEN:9265 (MONDO:equivalentTo)
  • UMLS:C0019624 (MONDO:equivalentTo)
  • DOID:4330 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, disease_grouping, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, harrisons_view_immune_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, mondo_top_grouping_immune_system_disorder, harrisons_view_member, ordo_group_of_disorders

exactMatch

http://identifiers.org/medgen/9265

http://identifiers.org/snomedct/127069007

http://purl.obolibrary.org/obo/DOID_4330

http://www.orpha.net/ORDO/Orphanet_157987

http://linkedlifedata.com/resource/umls/id/C0019624

http://identifiers.org/mesh/D015616

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0017368

has related synonym

histiocytosis, non-Langerhans-cell

id

MONDO:0015531

Term relations

Subclass of: