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subcutaneous panniculitis-like T-cell lymphoma

Go to external page http://purl.obolibrary.org/obo/MONDO_0019475

Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare cytotoxic cutaneous lymphoma that has been recognized as a distinct subset of peripheral T-cell lymphomas originating and presenting primarily in the subcutaneous fat tissue. [ Orphanet:86884 ]

Synonyms: subcutaneous panniculitis-like T-cell lymphoma, Alpha/Beta type subcutaneous panniculitis-like T-cell lymphoma SPTCL subcutaneous panniculitis-like T-cell lymphoma (Alpha/Beta type) subcutaneous panniculitic T-cell lymphoma

This is just here as a test because I lose it

Term information

database cross reference
  • ICDO:9708/3 (NCIT:C6918)
  • GARD:10193 (MONDO:GARD)
  • ICD10CM:C86.3 (MONDO:equivalentTo)
  • ONCOTREE:SPTCL (MONDO:equivalentTo)
  • EFO:1000552 (MONDO:equivalentTo)
  • MEDGEN:99306 (MONDO:equivalentTo)
  • NCIT:C6918 (MONDO:equivalentTo)
  • NANDO:2200030 (https://orcid.org/0000-0003-0011-764X)
  • MESH:C537503 (Orphanet:86884/e)
  • Orphanet:86884 (OMIM:618398)
  • icd11.foundation:1550338805 (Orphanet:86884)
  • UMLS:C0522624 (MONDO:equivalentTo)
  • OMIM:618398 (MONDO:equivalentTo)
  • ICD9:202.70 (MONDO:relatedTo)
  • SCTID:404133000 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, ordo_disorder, matrix_txgnn_grouping_cancer_or_benign_tumor, mondo_top_grouping_integumentary_system_disorder, matrix_llm__txgnn_other, mondo_top_grouping_member, harrisons_view_immune_system_disorder, nord_rare, matrix_included, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, rare, mondo_top_grouping_immune_system_disorder, orphanet_rare, harrisons_view_integumentary_system_disorder, 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, icd10_billable, harrisons_view_hematologic_disorder, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, harrisons_view_hereditary_disease

abbreviation
SPTCL [ https://omim.org/entry/618398 ONCOTREE:SPTCL Orphanet:86884 NCIT:C6918 ]

exactMatch

http://purl.bioontology.org/ontology/ICD10CM/C86.3

http://linkedlifedata.com/resource/umls/id/C0522624

http://identifiers.org/mesh/C537503

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1550338805

http://www.ebi.ac.uk/efo/EFO_1000552

http://identifiers.org/medgen/99306

http://www.orpha.net/ORDO/Orphanet_86884

https://omim.org/entry/618398

http://identifiers.org/snomedct/404133000

http://purl.obolibrary.org/obo/NCIT_C6918

has related synonym

T-CELL LYMPHOMA, SUBCUTANEOUS PANNICULITIS-LIKE

id

MONDO:0019475