An autoimmune disorder that manifests as different lupus-specific skin disorders; it can occur with systemic lupus erythematosus, or as a singular disease. [ NCIT:P378 ]
Term information
- SCTID:7119001 (MONDO:equivalentTo)
- DOID:0050169 (MONDO:equivalentTo)
- EFO:0003834 (MONDO:equivalentTo)
- icd11.foundation:1401395930 (MONDO:equivalentTo)
- MESH:D008178 (MONDO:equivalentTo)
- NCIT:C26819 (MONDO:equivalentTo)
- UMLS:C0024137 (MONDO:equivalentTo)
- GARD:6225 (MONDO:GARD)
- MEDGEN:7401 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, gard_rare, harrisons_view_connective_tissue_disorder, matrix_llm__is_glucose_dysfunction_other, matrix_txgnn_grouping_autoimmune_disease, otar, matrix_excluded, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, harrisons_view_immune_system_disorder, nord_rare, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, mondo_top_grouping_immune_system_disorder, rare, harrisons_view_member, mondo_top_grouping_connective_tissue_disorder
http://purl.obolibrary.org/obo/NCIT_C26819
http://identifiers.org/snomedct/7119001
http://purl.obolibrary.org/obo/DOID_0050169
http://identifiers.org/mesh/D008178
http://www.ebi.ac.uk/efo/EFO_0003834
http://identifiers.org/medgen/7401
http://linkedlifedata.com/resource/umls/id/C0024137
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1401395930