This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0079773 (MONDO:equivalentTo)
  • MEDGEN:36336 (MONDO:equivalentTo)
  • Orphanet:171901 (MONDO:equivalentTo)
  • GARD:6226 (MONDO:GARD)
  • MedDRA:10011677 (Orphanet:171901/e)
  • MESH:D016410 (Orphanet:171901/e)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_txgnn_grouping_cancer_or_benign_tumor, mondo_top_grouping_integumentary_system_disorder, disease_grouping, matrix_llm__txgnn_other, mondo_top_grouping_member, obsoletion_candidate, nord_rare, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, rare, harrisons_view_integumentary_system_disorder, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, mondo_top_grouping_hematologic_disorder, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, 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, ordo_group_of_disorders

closeMatch

http://identifiers.org/meddra/10011677

comment

Reason of obsoletion: duplicate. This will be merged with MONDO:0000607 primary cutaneous T-cell non-Hodgkin lymphoma

exactMatch

http://identifiers.org/medgen/36336

http://linkedlifedata.com/resource/umls/id/C0079773

http://www.orpha.net/ORDO/Orphanet_171901

id

MONDO:0015758

term tracker item

https://github.com/monarch-initiative/mondo/issues/8583