An autoimmune condition characterized by red, well-delineated plaques with silvery scales that are usually on the extensor surfaces and scalp. They can occasionally present with these manifestations: pustules; erythema and scaling in intertriginous areas, and erythroderma, that are often distributed on extensor surfaces and scalp. [ NCIT:P378 ]

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:696.8 (MONDO:relatedTo)
  • ICD9:696.5 (EFO:0000676)
  • SCTID:9014002 (MONDO:equivalentTo)
  • OMIMPS:177900 (https://orcid.org/0000-0002-6601-2165)
  • icd11.foundation:63698555 (MONDO:equivalentTo)
  • MEDGEN:10997 (MONDO:equivalentTo)
  • UMLS:C0033860 (MONDO:equivalentTo)
  • ICD9:696 (EFO:0000676)
  • EFO:0000676 (MONDO:equivalentTo)
  • ICD9:696.1 (MONDO:relatedTo)
  • NCIT:C3346 (MONDO:equivalentTo)
  • MESH:D011565 (MONDO:equivalentTo)
  • ICD10CM:L40 (MONDO:equivalentTo)
  • DOID:8893 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, mondo_top_grouping_integumentary_system_disorder, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, harrisons_view_immune_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_included, matrix_txgnn_grouping_other, harrisons_view_inflammatory_disease, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_immune_system_disorder, harrisons_view_member, mondo_top_grouping_inflammatory_disease, harrisons_view_hereditary_disease, harrisons_view_integumentary_system_disorder

contributor

https://orcid.org/0000-0002-1149-7767

https://orcid.org/0000-0003-2955-4640

exactMatch

http://identifiers.org/snomedct/9014002

http://www.ebi.ac.uk/efo/EFO_0000676

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/63698555

http://purl.bioontology.org/ontology/ICD10CM/L40

http://identifiers.org/mesh/D011565

http://purl.obolibrary.org/obo/NCIT_C3346

http://purl.obolibrary.org/obo/DOID_8893

http://linkedlifedata.com/resource/umls/id/C0033860

https://omim.org/phenotypicSeries/PS177900

http://identifiers.org/medgen/10997

id

MONDO:0005083

should conform to

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