A benign, darkly pigmented skin lesion characterized by proliferation of keratinocytes and melanocytes. [ NCIT:P378 ]

This is just here as a test because I lose it

Term information

database cross reference
  • DOID:11684 (MONDO:equivalentTo)
  • NCIT:C27548 (MONDO:equivalentTo)
  • UMLS:C1321683 (MONDO:equivalentTo)
  • Wikipedia:Melanocanthoma (EFO:1000733)
  • SCTID:394727000 (MONDO:equivalentTo)
  • EFO:1000733 (MONDO:equivalentTo)
  • MEDGEN:272110 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_integumentary_system_disorder, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, matrix_included, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, harrisons_view_hereditary_disease, mondo_top_grouping_disorder_of_development_or_morphogenesis, harrisons_view_integumentary_system_disorder

exactMatch

http://identifiers.org/snomedct/394727000

http://purl.obolibrary.org/obo/NCIT_C27548

http://identifiers.org/medgen/272110

http://purl.obolibrary.org/obo/DOID_11684

http://linkedlifedata.com/resource/umls/id/C1321683

http://www.ebi.ac.uk/efo/EFO_1000733

id

MONDO:0006579

Term relations

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