diff --git a/mappings/ari.equivalencies.tsv b/mappings/ari.equivalencies.tsv index b175561..a63456f 100644 --- a/mappings/ari.equivalencies.tsv +++ b/mappings/ari.equivalencies.tsv @@ -619,3 +619,78 @@ ARI 0001158 Polyglandular autoimmune syndrome type 2 skos:exactMatch DOID 006023 ARI 0001158 Polyglandular autoimmune syndrome type 2 skos:exactMatch umls C1275078 manual-negative github:KrishnaTO ARI 0001158 Polyglandular autoimmune syndrome type 2 skos:exactMatch mesh C563187 manual-negative github:KrishnaTO ARI 0001158 Polyglandular autoimmune syndrome type 2 skos:exactMatch ncit C98873 manual-negative github:KrishnaTO +ARI 0001166 Primary biliary cholangitis skos:exactMatch SNOMEDCT 31712002 manual github:KrishnaTO +ARI 0001166 Primary biliary cholangitis skos:exactMatch omop 4135822 manual github:KrishnaTO +ARI 0001166 Primary biliary cholangitis skos:exactMatch DOID 12236 manual github:KrishnaTO +ARI 0001166 Primary biliary cholangitis skos:exactMatch MONDO 0005388 manual github:KrishnaTO +ARI 0001166 Primary biliary cholangitis skos:exactMatch ncit C27167 manual github:KrishnaTO +ARI 0001166 Primary biliary cholangitis skos:exactMatch umls C0008312 manual github:KrishnaTO +ARI 0001166 Primary biliary cholangitis skos:exactMatch ORPHA 186 manual github:KrishnaTO +ARI 0001166 Primary biliary cholangitis skos:exactMatch icd10cm K74.3 manual github:KrishnaTO +ARI 0001166 Primary biliary cholangitis skos:exactMatch mesh D008105 manual github:KrishnaTO +ARI 0001190 SLE glomerulonephritis syndrome skos:exactMatch SNOMEDCT 68815009 manual github:KrishnaTO +ARI 0001190 SLE glomerulonephritis syndrome skos:exactMatch omop 4285717 manual github:KrishnaTO +ARI 0001190 SLE glomerulonephritis syndrome skos:exactMatch DOID 0080162 manual github:KrishnaTO +ARI 0001190 SLE glomerulonephritis syndrome skos:exactMatch MONDO 0005556 manual github:KrishnaTO +ARI 0001190 SLE glomerulonephritis syndrome skos:exactMatch ncit C34789 manual github:KrishnaTO +ARI 0001190 SLE glomerulonephritis syndrome skos:exactMatch umls C0024143 manual github:KrishnaTO +ARI 0001190 SLE glomerulonephritis syndrome skos:exactMatch mesh D008181 manual github:KrishnaTO +ARI 0001187 Schnitzler syndrome skos:exactMatch SNOMEDCT 402415001 manual github:KrishnaTO +ARI 0001187 Schnitzler syndrome skos:exactMatch omop 4297647 manual github:KrishnaTO +ARI 0001187 Schnitzler syndrome skos:exactMatch DOID 4371 manual github:KrishnaTO +ARI 0001187 Schnitzler syndrome skos:exactMatch MONDO 0018304 manual github:KrishnaTO +ARI 0001187 Schnitzler syndrome skos:exactMatch ORPHA 37748 manual github:KrishnaTO +ARI 0001187 Schnitzler syndrome skos:exactMatch umls C0524988 manual github:KrishnaTO +ARI 0001187 Schnitzler syndrome skos:exactMatch mesh D019873 manual github:KrishnaTO +ARI 0001191 Small fiber neuropathy skos:exactMatch SNOMEDCT 709489006 manual github:KrishnaTO +ARI 0001191 Small fiber neuropathy skos:exactMatch DOID 0070701 manual github:KrishnaTO +ARI 0001191 Small fiber neuropathy skos:exactMatch omop 46271378 manual github:KrishnaTO +ARI 0001191 Small fiber neuropathy skos:exactMatch MONDO 0800207 manual github:KrishnaTO +ARI 0001191 Small fiber neuropathy skos:exactMatch ncit C125389 manual github:KrishnaTO +ARI 0001191 Small fiber neuropathy skos:exactMatch umls C3276706 manual github:KrishnaTO +ARI 0001191 Small fiber neuropathy skos:exactMatch mesh D000071075 manual github:KrishnaTO +ARI 0001201 Temporal arteritis skos:exactMatch SNOMEDCT 400130008 manual github:KrishnaTO +ARI 0001201 Temporal arteritis skos:exactMatch omop 4290976 manual github:KrishnaTO +ARI 0001201 Temporal arteritis skos:exactMatch DOID 13375 manual github:KrishnaTO +ARI 0001201 Temporal arteritis skos:exactMatch MONDO 0008538 manual github:KrishnaTO +ARI 0001201 Temporal arteritis skos:exactMatch ncit C35065 manual github:KrishnaTO +ARI 0001201 Temporal arteritis skos:exactMatch umls C0039483 manual github:KrishnaTO +ARI 0001201 Temporal arteritis skos:exactMatch ORPHA 397 manual github:KrishnaTO +ARI 0001201 Temporal arteritis skos:exactMatch mesh D013700 manual github:KrishnaTO +ARI 0001203 Tolosa-Hunt syndrome skos:exactMatch SNOMEDCT 95794005 manual github:KrishnaTO +ARI 0001203 Tolosa-Hunt syndrome skos:exactMatch omop 4317989 manual github:KrishnaTO +ARI 0001203 Tolosa-Hunt syndrome skos:exactMatch DOID 1278 manual github:KrishnaTO +ARI 0001203 Tolosa-Hunt syndrome skos:exactMatch MONDO 0018983 manual github:KrishnaTO +ARI 0001203 Tolosa-Hunt syndrome skos:exactMatch ncit C85193 manual github:KrishnaTO +ARI 0001203 Tolosa-Hunt syndrome skos:exactMatch mesh D020333 manual github:KrishnaTO +ARI 0001203 Tolosa-Hunt syndrome skos:exactMatch umls C0040381 manual github:KrishnaTO +ARI 0001203 Tolosa-Hunt syndrome skos:exactMatch ORPHA 64686 manual github:KrishnaTO +ARI 0001206 Undifferentiated connective tissue disease skos:exactMatch SNOMEDCT 239918008 manual github:KrishnaTO +ARI 0001206 Undifferentiated connective tissue disease skos:exactMatch omop 4344165 manual github:KrishnaTO +ARI 0001206 Undifferentiated connective tissue disease skos:exactMatch MONDO 0019527 manual github:KrishnaTO +ARI 0001206 Undifferentiated connective tissue disease skos:exactMatch ncit C116776 manual github:KrishnaTO +ARI 0001206 Undifferentiated connective tissue disease skos:exactMatch mesh D000074079 manual github:KrishnaTO +ARI 0001206 Undifferentiated connective tissue disease skos:exactMatch umls C0409999 manual github:KrishnaTO +ARI 0001206 Undifferentiated connective tissue disease skos:exactMatch ORPHA 90002 manual github:KrishnaTO +ARI 0001207 Urticarial vasculitis skos:exactMatch SNOMEDCT 402656007 manual github:KrishnaTO +ARI 0001207 Urticarial vasculitis skos:exactMatch omop 4292532 manual github:KrishnaTO +ARI 0001166 Primary biliary cholangitis skos:exactMatch ncit C51225 manual-negative github:KrishnaTO +ARI 0001166 Primary biliary cholangitis skos:exactMatch umls C0023892 manual-negative github:KrishnaTO +ARI 0001166 Primary biliary cholangitis skos:exactMatch icd10cm K74.5 manual-negative github:KrishnaTO +ARI 0001207 Urticarial vasculitis skos:exactMatch MONDO 0018227 manual-negative github:KrishnaTO +ARI 0001207 Urticarial vasculitis skos:exactMatch ORPHA 36412 manual-negative github:KrishnaTO +ARI 0001207 Urticarial vasculitis skos:exactMatch umls C0343206 manual-negative github:KrishnaTO +ARI 0001190 SLE glomerulonephritis syndrome skos:exactMatch icd10cm NoTermFound manual-absent github:KrishnaTO +ARI 0001190 SLE glomerulonephritis syndrome skos:exactMatch ORPHA NoTermFound manual-absent github:KrishnaTO +ARI 0001187 Schnitzler syndrome skos:exactMatch ncit NoTermFound manual-absent github:KrishnaTO +ARI 0001187 Schnitzler syndrome skos:exactMatch icd10cm NoTermFound manual-absent github:KrishnaTO +ARI 0001191 Small fiber neuropathy skos:exactMatch ORPHA NoTermFound manual-absent github:KrishnaTO +ARI 0001191 Small fiber neuropathy skos:exactMatch icd10cm NoTermFound manual-absent github:KrishnaTO +ARI 0001203 Tolosa-Hunt syndrome skos:exactMatch icd10cm NoTermFound manual-absent github:KrishnaTO +ARI 0001206 Undifferentiated connective tissue disease skos:exactMatch DOID NoTermFound manual-absent github:KrishnaTO +ARI 0001207 Urticarial vasculitis skos:exactMatch DOID NoTermFound manual-absent github:KrishnaTO +ARI 0001207 Urticarial vasculitis skos:exactMatch MONDO NoTermFound manual-absent github:KrishnaTO +ARI 0001207 Urticarial vasculitis skos:exactMatch ncit NoTermFound manual-absent github:KrishnaTO +ARI 0001207 Urticarial vasculitis skos:exactMatch icd10cm NoTermFound manual-absent github:KrishnaTO +ARI 0001207 Urticarial vasculitis skos:exactMatch mesh NoTermFound manual-absent github:KrishnaTO +ARI 0001207 Urticarial vasculitis skos:exactMatch ORPHA NoTermFound manual-absent github:KrishnaTO diff --git a/mappings/ari.sssom.tsv b/mappings/ari.sssom.tsv index 24d6933..3b4fbec 100644 --- a/mappings/ari.sssom.tsv +++ b/mappings/ari.sssom.tsv @@ -640,3 +640,78 @@ ARI:0001158 Polyglandular autoimmune syndrome type 2 skos:exactMatch Not DOID:00 ARI:0001158 Polyglandular autoimmune syndrome type 2 skos:exactMatch Not umls:C1275078 umls semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T21:38:45+00:00 ARI:0001158 Polyglandular autoimmune syndrome type 2 skos:exactMatch Not mesh:C563187 mesh semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T21:38:45+00:00 ARI:0001158 Polyglandular autoimmune syndrome type 2 skos:exactMatch Not ncit:C98873 ncit semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T21:38:45+00:00 +ARI:0001166 Primary biliary cholangitis skos:exactMatch SNOMEDCT:31712002 SNOMEDCT semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001166 Primary biliary cholangitis skos:exactMatch omop:4135822 omop semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001166 Primary biliary cholangitis skos:exactMatch DOID:12236 DOID semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001166 Primary biliary cholangitis skos:exactMatch MONDO:0005388 MONDO semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001166 Primary biliary cholangitis skos:exactMatch ncit:C27167 ncit semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001166 Primary biliary cholangitis skos:exactMatch umls:C0008312 umls semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001166 Primary biliary cholangitis skos:exactMatch ORPHA:186 ORPHA semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001166 Primary biliary cholangitis skos:exactMatch icd10cm:K74.3 icd10cm semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001166 Primary biliary cholangitis skos:exactMatch mesh:D008105 mesh semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001190 SLE glomerulonephritis syndrome skos:exactMatch SNOMEDCT:68815009 SNOMEDCT semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001190 SLE glomerulonephritis syndrome skos:exactMatch omop:4285717 omop semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001190 SLE glomerulonephritis syndrome skos:exactMatch DOID:0080162 DOID semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001190 SLE glomerulonephritis syndrome skos:exactMatch MONDO:0005556 MONDO semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001190 SLE glomerulonephritis syndrome skos:exactMatch ncit:C34789 ncit semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001190 SLE glomerulonephritis syndrome skos:exactMatch umls:C0024143 umls semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001190 SLE glomerulonephritis syndrome skos:exactMatch mesh:D008181 mesh semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001187 Schnitzler syndrome skos:exactMatch SNOMEDCT:402415001 SNOMEDCT semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001187 Schnitzler syndrome skos:exactMatch omop:4297647 omop semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001187 Schnitzler syndrome skos:exactMatch DOID:4371 DOID semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001187 Schnitzler syndrome skos:exactMatch MONDO:0018304 MONDO semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001187 Schnitzler syndrome skos:exactMatch ORPHA:37748 ORPHA semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001187 Schnitzler syndrome skos:exactMatch umls:C0524988 umls semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001187 Schnitzler syndrome skos:exactMatch mesh:D019873 mesh semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001191 Small fiber neuropathy skos:exactMatch SNOMEDCT:709489006 SNOMEDCT semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001191 Small fiber neuropathy skos:exactMatch DOID:0070701 DOID semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001191 Small fiber neuropathy skos:exactMatch omop:46271378 omop semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001191 Small fiber neuropathy skos:exactMatch MONDO:0800207 MONDO semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001191 Small fiber neuropathy skos:exactMatch ncit:C125389 ncit semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001191 Small fiber neuropathy skos:exactMatch umls:C3276706 umls semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001191 Small fiber neuropathy skos:exactMatch mesh:D000071075 mesh semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001201 Temporal arteritis skos:exactMatch SNOMEDCT:400130008 SNOMEDCT semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001201 Temporal arteritis skos:exactMatch omop:4290976 omop semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001201 Temporal arteritis skos:exactMatch DOID:13375 DOID semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001201 Temporal arteritis skos:exactMatch MONDO:0008538 MONDO semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001201 Temporal arteritis skos:exactMatch ncit:C35065 ncit semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001201 Temporal arteritis skos:exactMatch umls:C0039483 umls semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001201 Temporal arteritis skos:exactMatch ORPHA:397 ORPHA semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001201 Temporal arteritis skos:exactMatch mesh:D013700 mesh semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001203 Tolosa-Hunt syndrome skos:exactMatch SNOMEDCT:95794005 SNOMEDCT semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001203 Tolosa-Hunt syndrome skos:exactMatch omop:4317989 omop semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001203 Tolosa-Hunt syndrome skos:exactMatch DOID:1278 DOID semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001203 Tolosa-Hunt syndrome skos:exactMatch MONDO:0018983 MONDO semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001203 Tolosa-Hunt syndrome skos:exactMatch ncit:C85193 ncit semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001203 Tolosa-Hunt syndrome skos:exactMatch mesh:D020333 mesh semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001203 Tolosa-Hunt syndrome skos:exactMatch umls:C0040381 umls semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001203 Tolosa-Hunt syndrome skos:exactMatch ORPHA:64686 ORPHA semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001206 Undifferentiated connective tissue disease skos:exactMatch SNOMEDCT:239918008 SNOMEDCT semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001206 Undifferentiated connective tissue disease skos:exactMatch omop:4344165 omop semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001206 Undifferentiated connective tissue disease skos:exactMatch MONDO:0019527 MONDO semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001206 Undifferentiated connective tissue disease skos:exactMatch ncit:C116776 ncit semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001206 Undifferentiated connective tissue disease skos:exactMatch mesh:D000074079 mesh semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001206 Undifferentiated connective tissue disease skos:exactMatch umls:C0409999 umls semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001206 Undifferentiated connective tissue disease skos:exactMatch ORPHA:90002 ORPHA semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001207 Urticarial vasculitis skos:exactMatch SNOMEDCT:402656007 SNOMEDCT semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001207 Urticarial vasculitis skos:exactMatch omop:4292532 omop semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001166 Primary biliary cholangitis skos:exactMatch Not ncit:C51225 ncit semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001166 Primary biliary cholangitis skos:exactMatch Not umls:C0023892 umls semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001166 Primary biliary cholangitis skos:exactMatch Not icd10cm:K74.5 icd10cm semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001207 Urticarial vasculitis skos:exactMatch Not MONDO:0018227 MONDO semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001207 Urticarial vasculitis skos:exactMatch Not ORPHA:36412 ORPHA semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001207 Urticarial vasculitis skos:exactMatch Not umls:C0343206 umls semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001190 SLE glomerulonephritis syndrome skos:exactMatch sssom:NoTermFound icd10cm semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001190 SLE glomerulonephritis syndrome skos:exactMatch sssom:NoTermFound ORPHA semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001187 Schnitzler syndrome skos:exactMatch sssom:NoTermFound ncit semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001187 Schnitzler syndrome skos:exactMatch sssom:NoTermFound icd10cm semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001191 Small fiber neuropathy skos:exactMatch sssom:NoTermFound ORPHA semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001191 Small fiber neuropathy skos:exactMatch sssom:NoTermFound icd10cm semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001203 Tolosa-Hunt syndrome skos:exactMatch sssom:NoTermFound icd10cm semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001206 Undifferentiated connective tissue disease skos:exactMatch sssom:NoTermFound DOID semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001207 Urticarial vasculitis skos:exactMatch sssom:NoTermFound DOID semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001207 Urticarial vasculitis skos:exactMatch sssom:NoTermFound MONDO semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001207 Urticarial vasculitis skos:exactMatch sssom:NoTermFound ncit semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001207 Urticarial vasculitis skos:exactMatch sssom:NoTermFound icd10cm semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001207 Urticarial vasculitis skos:exactMatch sssom:NoTermFound mesh semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 +ARI:0001207 Urticarial vasculitis skos:exactMatch sssom:NoTermFound ORPHA semapv:ManualMappingCuration github:KrishnaTO 2026-09-07T23:44:41+00:00 diff --git a/ontologies/ari_t1d.owl b/ontologies/ari_t1d.owl index 4576335..13810af 100644 --- a/ontologies/ari_t1d.owl +++ b/ontologies/ari_t1d.owl @@ -17839,7 +17839,6 @@ To date, there is no direct or indirect evidence that post-pericardiotomy syndro - @@ -17858,31 +17857,34 @@ To date, there is no direct or indirect evidence that post-pericardiotomy syndro + + Primary biliary cholangitis is chronic disease in which the bile ducts of the liver are slowly destroyed due to inflammation with progressive scarring. Primary biliary cholangitis - false + Antibody + Autoimmune + 125887.0 + 30-60 years ARI:0001166 + PBC + Primary biliary cirrhosis + 2 + 2026-06-15 10:37 | Importer | Imported from ARI core reports + 2026-09-07T23:44:38+00:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 31712002; confirmed OMOP 4135822; confirmed DOID 12236; confirmed MONDO 0005388; confirmed NCI C27167; confirmed UMLS C0008312; confirmed ORPHANET 186; confirmed ICD10 K74.3; confirmed MESH D008105; flagged NCI C51225; flagged UMLS C0023892; flagged ICD10 K74.5 + 2026-09-07T23:44:38+00:00 | KrishnaTO | Stored confirmed cross-reference: MONDO 0005388; ORPHANET 186 + 2026-09-07T23:44:38+00:00 | KrishnaTO | Removed flagged cross-reference: NCI C51225; UMLS C0023892; ICD10 K74.5 31712002 12236 - C0023892 C0008312 + 0005388 K74.3 - K74.5 - D008105 - C27167 - C51225 + Female 110793/100k; Male 15094/100k; F:M ratio 7.3402 + https://pubmed.ncbi.nlm.nih.gov/29066370/ + Lu 2017; https://pubmed.ncbi.nlm.nih.gov/29066370/ + false 4135822 31712002 - Primary biliary cholangitis is chronic disease in which the bile ducts of the liver are slowly destroyed due to inflammation with progressive scarring. - PBC - Primary biliary cirrhosis - Lu 2017; https://pubmed.ncbi.nlm.nih.gov/29066370/ - https://pubmed.ncbi.nlm.nih.gov/29066370/ - Antibody - Autoimmune - 2 - 125887.0 - Female 110793/100k; Male 15094/100k; F:M ratio 7.3402 - 30-60 years + D008105 + C27167 Canadian PBC Society | https://pbc-society.ca/ American Liver Foundation | https://liverfoundation.org/ Living With PBC | https://www.livingwithpbc.com/ @@ -17891,12 +17893,12 @@ To date, there is no direct or indirect evidence that post-pericardiotomy syndro PBC Foundation UK | https://www.pbcfoundation.org.uk/ Link to Healthline | https://www.healthline.com/health/primary-biliary-cirrhosis Link to Mayo Clinic | https://www.mayoclinic.org/diseases-conditions/primary-biliary-cholangitis/symptoms-causes/syc-20376874 - PBC, Early - Asymptomatic with elevated liver enzymes. - PBC, Advanced - Significant liver scarring and cirrhosis. Autoimmune Registry 2024-09 + PBC, Early - Asymptomatic with elevated liver enzymes. + PBC, Advanced - Significant liver scarring and cirrhosis. PBC - 2026-06-15 10:37 | Importer | Imported from ARI core reports + 186 @@ -20315,7 +20317,6 @@ Sarcoidosis often starts with a set of symptoms collectively referred to as Lofg - @@ -20324,37 +20325,42 @@ Sarcoidosis often starts with a set of symptoms collectively referred to as Lofg - Schnitzler syndrome - false - ARI:0001187 - 402415001 - 4371 - C0524988 - D019873 - 4297647 - 402415001 + Schnitzler syndrome is a disease in which periodic episodes of inflammation occur. It is considered an autoinflammatory disease, not an autoimmune disease, because the immune system does not mistakenly attack healthy cells. Instead, Schnitzler syndrome is believed to arise from a problem with the immune system itself. It is uncertain what causes Schnitzler syndrome, but it does not appear to be hereditary. Patients with Schnitzler syndrome typically experience chronic rash, relapsing fevers, pain and inflammation in the joints, enlarged lymph nodes, and an excess of certain proteins in the blood. The condition is chronic, generally without worsening, though 10-15% of people with Schnitzler syndrome experience cancerous or non-cancerous overproduction of certain types of white blood cells. There is no cure, but treatments may relieve symptoms in some individuals. + Schnitzler syndrome + Unconfirmed + Unconfirmed + 76.0 + 51-51 years + ARI:0001187 Chronic urticaria with gammopathy Chronic urticaria with gammapathy Chronic urticaria with macroglobulinemia Schnitzler's syndrome - de Koning 2014; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405827/ - Unconfirmed - Unconfirmed 2 - 76.0 + 2026-06-15 10:37 | Importer | Imported from ARI core reports + 2026-09-07T23:44:38+00:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 402415001; confirmed OMOP 4297647; confirmed DOID 4371; confirmed MONDO 0018304; confirmed ORPHANET 37748; confirmed UMLS C0524988; confirmed MESH D019873; no term in NCI; no term in ICD10 + 2026-09-07T23:44:38+00:00 | KrishnaTO | Stored confirmed cross-reference: MONDO 0018304; ORPHANET 37748 + 402415001 + 4371 + C0524988 + 0018304 Male 76/100k - 51-51 years + de Koning 2014; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405827/ + false + 4297647 + 402415001 + D019873 Autoinflammatory Alliance | http://www.nomidalliance.org/schnitzler.php Schnitzler's Syndrome Awareness Group | https://www.facebook.com/groups/762965077115305/ Systemic Autoinflammatory Disease (SAID) Support | http://saidsupport.org/ - Schnitzler Syndrome, Classic - Chronic urticaria, fever, and monoclonal gammopathy. Emily Romanello | https://www.linkedin.com/in/emily-romanello-1392432a 2024-09 + Schnitzler Syndrome, Classic - Chronic urticaria, fever, and monoclonal gammopathy. SCH - 2026-06-15 10:37 | Importer | Imported from ARI core reports + 37748 @@ -20736,7 +20742,6 @@ Patients with Schnitzler syndrome typically experience chronic rash, relapsing f - @@ -20756,21 +20761,28 @@ Patients with Schnitzler syndrome typically experience chronic rash, relapsing f + + Lupus nephritis is a complication in patients with systemic lupus erythematosus (SLE), an autoimmune condition causing inflammation of the body's tissues. Lupus nephritis targets the kidneys, causing damage and inflammation, which prevents normal function and may lead to kidney failure. Significant delay or lack of treatment can be fatal, but early medical care can manage symptoms and result in a good prognosis. SLE glomerulonephritis syndrome - false + Antibody + Autoimmune + Can occur at any age. ARI:0001190 + Lupus nephritis + 2 + 2026-06-15 10:37 | Importer | Imported from ARI core reports + 2026-09-07T23:44:38+00:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 68815009; confirmed OMOP 4285717; confirmed DOID 0080162; confirmed MONDO 0005556; confirmed NCI C34789; confirmed UMLS C0024143; confirmed MESH D008181; no term in ICD10; no term in ORPHANET + 2026-09-07T23:44:38+00:00 | KrishnaTO | Stored confirmed cross-reference: MONDO 0005556; NCI C34789; UMLS C0024143 68815009 0080162 - D008181 + C0024143 + 0005556 + Wang 2017; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864167/ + false 4285717 68815009 - Lupus nephritis is a complication in patients with systemic lupus erythematosus (SLE), an autoimmune condition causing inflammation of the body's tissues. Lupus nephritis targets the kidneys, causing damage and inflammation, which prevents normal function and may lead to kidney failure. Significant delay or lack of treatment can be fatal, but early medical care can manage symptoms and result in a good prognosis. - Lupus nephritis - Wang 2017; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864167/ - Antibody - Autoimmune - 2 - Can occur at any age. + D008181 + C34789 Link to Cleveland Clinic | https://my.clevelandclinic.org/health/diseases/21809-lupus-nephritis Despite Lupus | http://despitelupus.blogspot.com/ Link to Healthline | https://www.healthline.com/health/lupus-nephritis @@ -20779,16 +20791,15 @@ Patients with Schnitzler syndrome typically experience chronic rash, relapsing f LupusChick | http://www.lupuschick.com/ Lupus and Allied Diseases Association | https://www.ladainc.org/ Lupus Foundation of America | https://www.lupus.org/ + Salma Fleifil + 2024-09 Lupus Nephritis, Class I (Minimal Mesangial) - Mild, no significant kidney damage. Lupus Nephritis, Class V (Membranous) - Protein leakage in urine. Lupus Nephritis, Class III (Focal) - Scattered inflammation with possible kidney function loss. Lupus Nephritis, Class II (Mesangial Proliferative) - More inflammation but mild symptoms. Lupus Nephritis, Class IV (Diffuse) - Severe kidney damage. Lupus Nephritis, Class VI (Advanced Sclerosis) - End-stage kidney disease. - Salma Fleifil - 2024-09 LN - 2026-06-15 10:37 | Importer | Imported from ARI core reports @@ -20908,19 +20919,22 @@ Patients with Schnitzler syndrome typically experience chronic rash, relapsing f + 1 Small fiber neuropathy - false ARI:0001191 + 2.1 + 2026-06-15 10:37 | Importer | Imported from ARI core reports + 2026-09-07T23:44:38+00:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 709489006; confirmed DOID 0070701; confirmed OMOP 46271378; confirmed MONDO 0800207; confirmed NCI C125389; confirmed UMLS C3276706; confirmed MESH D000071075; no term in ORPHANET; no term in ICD10 + 2026-09-07T23:44:38+00:00 | KrishnaTO | Stored confirmed cross-reference: MONDO 0800207 709489006 0070701 C3276706 + 0800207 + 1 million + false + 46271378 D000071075 C125389 - 46271378 - 1 - 1 million - 2.1 - 2026-06-15 10:37 | Importer | Imported from ARI core reports @@ -22333,7 +22347,6 @@ Early symptoms may include fever, night sweats, fatigue, joint pain, and chest d - @@ -22355,38 +22368,45 @@ Early symptoms may include fever, night sweats, fatigue, joint pain, and chest d + + Temporal arteritis, also known as giant cell arteritis, is an inflammation of the lining of the arteries that typically affects the arteries in the head. Temporal arteritis can frequently cause headaches, scalp tenderness, jaw pain and vision problems. Temporal arteritis - false + TCELL + Autoimmune + 50-100 years ARI:0001201 - 400130008 - 13375 - C0039483 - D013700 - C35065 - 4290976 - 400130008 - Temporal arteritis, also known as giant cell arteritis, is an inflammation of the lining of the arteries that typically affects the arteries in the head. Temporal arteritis can frequently cause headaches, scalp tenderness, jaw pain and vision problems. GCA Horton's disease Cranial arteritis Giant cell arteritis Granulomatous arteritis - Crowson 2017; https://pubmed.ncbi.nlm.nih.gov/28551169/ - https://pubmed.ncbi.nlm.nih.gov/28551169/ - TCELL - Autoimmune 2 - 50-100 years + 2026-06-15 10:37 | Importer | Imported from ARI core reports + 2026-09-07T23:11:29+00:00 | user | Edited: icd10 + 2026-09-07T23:44:38+00:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 400130008; confirmed OMOP 4290976; confirmed DOID 13375; confirmed MONDO 0008538; confirmed NCI C35065; confirmed UMLS C0039483; confirmed ORPHANET 397; confirmed MESH D013700 + 2026-09-07T23:44:38+00:00 | KrishnaTO | Stored confirmed cross-reference: MONDO 0008538; ORPHANET 397 + 400130008 + 13375 + C0039483 + 0008538 + M31.6 + https://pubmed.ncbi.nlm.nih.gov/28551169/ + Crowson 2017; https://pubmed.ncbi.nlm.nih.gov/28551169/ + false + 4290976 + 400130008 + D013700 + C35065 Link to Healthline | https://www.healthline.com/health/temporal-arteritis Link to Cleveland Clinic | https://my.clevelandclinic.org/health/diseases/temporal-arteritis-giant-cell-arteritis Vasculitis Foundation | https://www.vasculitisfoundation.org/ Link to Mayo Clinic | https://www.mayoclinic.org/diseases-conditions/giant-cell-arteritis/symptoms-causes/syc-20372758 - Temporal Arteritis, Large Vessel - Involves the aorta and major arteries. - Temporal Arteritis, Cranial - Affects the head, causing headache and vision loss. Autoimmune Registry 2024-09 + Temporal Arteritis, Large Vessel - Involves the aorta and major arteries. + Temporal Arteritis, Cranial - Affects the head, causing headache and vision loss. TA - 2026-06-15 10:37 | Importer | Imported from ARI core reports + 397 @@ -22529,39 +22549,43 @@ Early symptoms may include fever, night sweats, fatigue, joint pain, and chest d - + + Patients with Tolosa-Hunt syndrome experience episodes of severe headaches surrounding the eyes, along with restricted eye movement that is painful (ophthalmoplegia). Normally, only one eye is affected and will frequently appear protruded. Symptoms may also include nerve abnormalities, such as eyelid drooping, double vision, large pupil, and numbness of the face. This disorder typically occurs in relapsing flares. The cause of Tolosa-Hunt syndrome is unknown but is associated with the inflammation within the eyes and may be autoimmune. Tolosa-Hunt syndrome - false + Unconfirmed + Unconfirmed ARI:0001203 - 95794005 - 1278 - C0040381 - D020333 - C85193 - 4317989 - 95794005 - Patients with Tolosa-Hunt syndrome experience episodes of severe headaches surrounding the eyes, along with restricted eye movement that is painful (ophthalmoplegia). Normally, only one eye is affected and will frequently appear protruded. Symptoms may also include nerve abnormalities, such as eyelid drooping, double vision, large pupil, and numbness of the face. This disorder typically occurs in relapsing flares. The cause of Tolosa-Hunt syndrome is unknown but is associated with the inflammation within the eyes and may be autoimmune. Painful Ophthalmoplegia THS Non-specific inflammation of the superior orbital fissure Non-specific inflammation of the cavernous sinus - Iaconetta 2005; https://pubmed.ncbi.nlm.nih.gov/16109058/ - https://pubmed.ncbi.nlm.nih.gov/16109058/ - Unconfirmed - Unconfirmed 2 + 2026-06-15 10:37 | Importer | Imported from ARI core reports + 2026-09-07T23:44:38+00:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 95794005; confirmed OMOP 4317989; confirmed DOID 1278; confirmed MONDO 0018983; confirmed NCI C85193; confirmed MESH D020333; confirmed UMLS C0040381; confirmed ORPHANET 64686; no term in ICD10 + 2026-09-07T23:44:38+00:00 | KrishnaTO | Stored confirmed cross-reference: MONDO 0018983; ORPHANET 64686 + 95794005 + 1278 + C0040381 + 0018983 + https://pubmed.ncbi.nlm.nih.gov/16109058/ + Iaconetta 2005; https://pubmed.ncbi.nlm.nih.gov/16109058/ + false + 4317989 + 95794005 + D020333 + C85193 Link to Cleveland Clinic | https://my.clevelandclinic.org/health/diseases/25233-tolosa-hunt-syndrome Tolosa-Hunt Syndrome Support Page | https://www.facebook.com/pg/tolosahuntsyndrome/ - Tolosa-Hunt Syndrome, Classic - Painful ophthalmoplegia due to cavernous sinus inflammation. Autoimmune Registry 2024-09 + Tolosa-Hunt Syndrome, Classic - Painful ophthalmoplegia due to cavernous sinus inflammation. THA - 2026-06-15 10:37 | Importer | Imported from ARI core reports + 64686 @@ -22965,7 +22989,6 @@ Both UC and CD are caused by an autoimmune response that reflects the involvemen - @@ -22985,31 +23008,41 @@ Both UC and CD are caused by an autoimmune response that reflects the involvemen + + Patients of undifferentiated connective tissue disease (UCTD) share some, but not all, symptoms with other connective tissue diseases, such as systemic lupus erythmatosus, systemic sclerosis, dermatomyositis, polymyositis, rheumatoid arthritis, Sjogren's syndrome, and antiphospholipid syndrome. UCTD is diagnosed when a patient has a positive serum ANA test and shows stable symptoms for a minimum of 3 years. UCTD is distinct from the other above-mentioned diseases in that the condition remains stable over time without worsening. 30% of patients diagnosed with UCTD will be given a new diagnosis because their disease will not remain stable. Undifferentiated connective tissue disease - false + Unconfirmed + Unconfirmed + 153.0 + 30-50 years ARI:0001206 - 239918008 - 4344165 - 239918008 - Patients of undifferentiated connective tissue disease (UCTD) share some, but not all, symptoms with other connective tissue diseases, such as systemic lupus erythmatosus, systemic sclerosis, dermatomyositis, polymyositis, rheumatoid arthritis, Sjogren's syndrome, and antiphospholipid syndrome. UCTD is diagnosed when a patient has a positive serum ANA test and shows stable symptoms for a minimum of 3 years. UCTD is distinct from the other above-mentioned diseases in that the condition remains stable over time without worsening. 30% of patients diagnosed with UCTD will be given a new diagnosis because their disease will not remain stable. Undifferentiated connective tissue syndrome UCTD - Spinillo 2017; https://pubmed.ncbi.nlm.nih.gov/28921728/ - https://pubmed.ncbi.nlm.nih.gov/28921728/ - Unconfirmed - Unconfirmed 2 - 153.0 + 2026-06-15 10:37 | Importer | Imported from ARI core reports + 2026-09-07T23:29:56+00:00 | user | Edited: icd10 + 2026-09-07T23:44:38+00:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 239918008; confirmed OMOP 4344165; confirmed MONDO 0019527; confirmed NCI C116776; confirmed MESH D000074079; confirmed UMLS C0409999; confirmed ORPHANET 90002; no term in DOID + 2026-09-07T23:44:38+00:00 | KrishnaTO | Stored confirmed cross-reference: MONDO 0019527; NCI C116776; MESH D000074079; UMLS C0409999; ORPHANET 90002 + 239918008 + C0409999 + 0019527 + M35.9 Female 153/100k - 30-50 years + https://pubmed.ncbi.nlm.nih.gov/28921728/ + Spinillo 2017; https://pubmed.ncbi.nlm.nih.gov/28921728/ + false + 4344165 + 239918008 + D000074079 + C116776 Link to Cleveland Clinic | https://my.clevelandclinic.org/health/diseases/14803-connective-tissue-diseases Link to Healthline | https://www.healthline.com/health/undifferentiated-connective-tissue-disease - UCTD, Evolving - May develop into lupus or another connective tissue disorder. - UCTD, Stable - Persistent but does not progress into a defined autoimmune disease. Emily Romanello | https://www.linkedin.com/in/emily-romanello-1392432a 2024-09 + UCTD, Evolving - May develop into lupus or another connective tissue disorder. + UCTD, Stable - Persistent but does not progress into a defined autoimmune disease. UCTD - 2026-06-15 10:37 | Importer | Imported from ARI core reports + 90002 @@ -23128,7 +23161,6 @@ Both UC and CD are caused by an autoimmune response that reflects the involvemen - @@ -23147,27 +23179,31 @@ Both UC and CD are caused by an autoimmune response that reflects the involvemen - Urticarial vasculitis - false - ARI:0001207 - 402656007 - 4292532 - 402656007 + Autoimmune urticaria occurs when the immune system attacks the normal tissues of the body, resulting in hives. The condition becomes chronic when the lesions persists longer than 6 weeks. Chronic autoimmune urticaria has been found to be associated with autoimmune thyroid disease. Urticaria can also be caused by allergic reaction to plants like poison ivy, dyes found in clothing, and cosmetics. An allergic reaction is not an autoimmune disease because there is no involvement by the adaptive immune system and auto-antibodies that attack your own cells are not involved. There are antibodies (IgE antibodies), but they target the invading molecules (e.g., poison ivy), not the cells in the skin. In autoimmune urticaria, the antibodies created are attacking the skin itself, not an invading molecule. - Kolkhir 2020; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063238/ + Urticarial vasculitis Antibody Autoimmune - 2 Can occur at any age. + ARI:0001207 + 2 + 2026-06-15 10:37 | Importer | Imported from ARI core reports + 2026-09-07T23:38:17+00:00 | user | Edited: umls + 2026-09-07T23:44:38+00:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 402656007; confirmed OMOP 4292532; flagged MONDO 0018227; flagged ORPHANET 36412; flagged UMLS C0343206; no term in DOID; no term in MONDO; no term in NCI; no term in ICD10; no term in MESH; no term in ORPHANET + 402656007 + C1304408 + Kolkhir 2020; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063238/ + false + 4292532 + 402656007 Link to Cleveland Clinic | https://my.clevelandclinic.org/health/diseases/25204-urticarial-vasculitis - Urticarial Vasculitis, Normocomplementemic - Mild, normal complement levels. - Urticarial Vasculitis, Hypocomplementemic - More severe, with low complement levels. Suhani Dalal 2024-09 + Urticarial Vasculitis, Normocomplementemic - Mild, normal complement levels. + Urticarial Vasculitis, Hypocomplementemic - More severe, with low complement levels. URTV - 2026-06-15 10:37 | Importer | Imported from ARI core reports