A rare entity characterized by localized but destructive growth of a tumor consisting of highly atypical, immature mast cells.(WHO, 2001) [ NCIT:C9348 ]

Synonyms: mast-cell sarcoma sarcoma of mast cell MCS mast cell sarcoma

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C9348 (MONDO:equivalentTo)
  • icd11.foundation:1993363632 (MONDO:equivalentTo)
  • Orphanet:66661 (MONDO:equivalentTo)
  • icd11.foundation:233404891 (Orphanet:66661)
  • UMLS:C0036221 (MONDO:equivalentTo)
  • MESH:D012515 (Orphanet:66661/e)
  • EFO:1000364 (MONDO:equivalentTo)
  • DOID:355 (MONDO:equivalentTo)
  • ONCOTREE:MCSL (MONDO:equivalentTo)
  • SCTID:118615008 (MONDO:equivalentTo)
  • ICD9:202.6 (DOID:355)
  • MEDGEN:11322 (MONDO:equivalentTo)
  • GARD:18870 (MONDO:GARD)
  • ICDO:9740/3 (NCIT:C9348)
Subsets

matrix_llm__is_cancer_other, ordo_disorder, gard_rare, matrix_txgnn_grouping_cancer_or_benign_tumor, mondo_top_grouping_member, matrix_llm__txgnn_other, harrisons_view_immune_system_disorder, matrix_included, nord_rare, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, mondo_top_grouping_immune_system_disorder, rare, orphanet_rare, matrix_llm__is_glucose_dysfunction_other, otar, mondo_top_grouping_hematologic_disorder, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_hematologic_disorder, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, harrisons_view_hereditary_disease

abbreviation
MCSL [ ONCOTREE:MCSL ]

abbreviation
MCS [ NCIT:C9348 ]

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/sarcoma.yaml

exactMatch

http://purl.obolibrary.org/obo/NCIT_C9348

http://linkedlifedata.com/resource/umls/id/C0036221

http://identifiers.org/snomedct/118615008

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/233404891

http://identifiers.org/mesh/D012515

http://www.ebi.ac.uk/efo/EFO_1000364

http://identifiers.org/medgen/11322

http://purl.obolibrary.org/obo/DOID_355

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1993363632

http://www.orpha.net/ORDO/Orphanet_66661

id

MONDO:0019024