diff --git a/mappings/ari.equivalencies.tsv b/mappings/ari.equivalencies.tsv
index 8b41707..70515d7 100644
--- a/mappings/ari.equivalencies.tsv
+++ b/mappings/ari.equivalencies.tsv
@@ -500,3 +500,4 @@ ARI 0001143 Neuromyelitis optica skos:exactMatch icd10cm G36.0 manual github:aar
ARI 0001143 Neuromyelitis optica skos:exactMatch ORPHA 71211 manual github:aaronabend
ARI 0001143 Neuromyelitis optica skos:exactMatch mesh D009471 manual github:aaronabend
ARI 0001143 Neuromyelitis optica skos:exactMatch OMIM NoTermFound manual-absent github:aaronabend
+ARI 0001056 Birdshot chorioretinopathy skos:exactMatch ORPHA 179 manual github:KrishnaTO
diff --git a/mappings/ari.sssom.tsv b/mappings/ari.sssom.tsv
index 7f98369..03784d6 100644
--- a/mappings/ari.sssom.tsv
+++ b/mappings/ari.sssom.tsv
@@ -520,3 +520,4 @@ ARI:0001143 Neuromyelitis optica skos:exactMatch icd10cm:G36.0 icd10cm semapv:M
ARI:0001143 Neuromyelitis optica skos:exactMatch ORPHA:71211 ORPHA semapv:ManualMappingCuration github:aaronabend 2026-08-17
ARI:0001143 Neuromyelitis optica skos:exactMatch mesh:D009471 mesh semapv:ManualMappingCuration github:aaronabend 2026-08-17
ARI:0001143 Neuromyelitis optica skos:exactMatch sssom:NoTermFound OMIM semapv:ManualMappingCuration github:aaronabend 2026-08-17
+ARI:0001056 Birdshot chorioretinopathy skos:exactMatch ORPHA:179 ORPHA semapv:ManualMappingCuration github:KrishnaTO 2026-08-20
diff --git a/ontologies/ari_t1d.owl b/ontologies/ari_t1d.owl
index fec2fa2..d327d73 100644
--- a/ontologies/ari_t1d.owl
+++ b/ontologies/ari_t1d.owl
@@ -3653,27 +3653,7 @@ The trigger for antisynthetase syndrome is unknown, but it may be associated wit
2024-04
APA
2026-06-15 10:37 | Importer | Imported from ARI core reports
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: confirmed SNOMED 306058006; confirmed OMOP 137829; confirmed DOID 12449; confirmed MONDO 0015909; confirmed NCI C2870; confirmed ICD10 D61.9; confirmed OMIM 609135; confirmed UMLS C0002874; confirmed MESH D000741; flagged ORPHANET 182040
- Aplastic Anemias
- Aplastic anemia, unspecified
- Aplastic Anaemia
- Anemia, Aplastic
- Aplastic Anaemias
- Anaemia, Aplastic
- idiopathic aplastic anemia - subtype of Aplastic anemia (MONDO:0012197)
- Recurrent Aplastic Anemia - subtype of Aplastic anemia (NCIT:C153293)
- acquired aplastic anemia - subtype of Aplastic anemia (MONDO:0015610)
- congenital hypoplastic anemia - subtype of Aplastic anemia (DOID:1342)
- Aplastic Anemia due to Infection - subtype of Aplastic anemia (NCIT:C35466)
- Severe Aplastic Anemia - subtype of Aplastic anemia (NCIT:C61229)
- inherited aplastic anemia - subtype of Aplastic anemia (MONDO:0001713)
- myelophthisic anemia - subtype of Aplastic anemia (MONDO:0005868)
- Very Severe Aplastic Anemia - subtype of Aplastic anemia (NCIT:C173788)
- Non-Severe Aplastic Anemia - subtype of Aplastic anemia (NCIT:C173789)
- Aplastic Anemia due to Radiation - subtype of Aplastic anemia (NCIT:C35465)
- Drug/Toxin-Induced Aplastic Anemia - subtype of Aplastic anemia (NCIT:C70613)
- Drug-Induced Aplastic Anemia - subtype of Aplastic anemia (NCIT:C35343)
- 2026-08-18 00:06 | KrishnaTO | Enrichment from confirmed cross-references: +6 synonym(s), +13 clinical subtype(s)
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: confirmed SNOMED 306058006; confirmed OMOP 137829; confirmed DOID 12449; confirmed MONDO 0015909; confirmed NCI C2870; confirmed ICD10 D61.9; confirmed OMIM 609135; confirmed UMLS C0002874; confirmed MESH D000741; flagged ORPHANET 182040
@@ -6263,6 +6243,7 @@ Cicatricial pemphigoid is usually not chronic, and most patients symptoms disapp
Autoimmune
2
2026-06-15 10:37 | Importer | Imported from ARI core reports
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: confirmed ORPHANET 179
@@ -6466,26 +6447,7 @@ The first reports of narcolepsy being an autoimmune disease came in 2013, but re
2026-08-12 01:11 | KrishnaTO | Cross-reference review: confirmed SNOMED 193042000; confirmed OMOP 437854; confirmed MONDO 0016158; confirmed ICD10 G47.411; confirmed ORPHANET 2073; confirmed UMLS C0751362; flagged SNOMED 735676003; flagged OMOP 42536721
193042000
437854
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: confirmed NCI C196015; confirmed OMIM 161400; confirmed MESH D009290; flagged DOID 8986; no term in DOID
- Narcoleptic Syndrome
- Syndrome, Gelineau's
- Syndromes, Gelineau's
- Syndromes, Narcoleptic
- Gelineau's Syndromes
- Gelineaus Syndrome
- paroxysmal sleep
- Syndrome, Narcoleptic
- Sleep, Paroxysmal
- narcolepsy
- Narcoleptic Syndromes
- narcolepsy with or without cataplexy
- Syndrome, Gelineau
- Narcolepsy, without cataplexy
- Gelineau Syndrome
- Gelineau's Syndrome
- hereditary narcolepsy - subtype of Cataplexy and narcolepsy (MONDO:0100554)
- narcolepsy-cataplexy syndrome - subtype of Cataplexy and narcolepsy (MONDO:0016158)
- 2026-08-18 00:06 | KrishnaTO | Enrichment from confirmed cross-references: +16 synonym(s), +2 clinical subtype(s)
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: confirmed NCI C196015; confirmed OMIM 161400; confirmed MESH D009290; flagged DOID 8986; no term in DOID
@@ -6868,7 +6830,7 @@ The cause of this syndrome is unknown, however, researchers believe that it may
2026-08-03 18:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 52702003; confirmed OMOP 432738; confirmed DOID 8544; confirmed MONDO 0005404; confirmed NCI C3037; confirmed ICD10 G93.32; confirmed ORPHANET 1983; confirmed UMLS C0015674; confirmed MESH D015673; flagged ICD10 780.71
2026-08-03 18:15 | KrishnaTO | Cross-reference review: confirmed SNOMED 52702003; confirmed OMOP 432738; confirmed DOID 8544; confirmed MONDO 0005404; confirmed NCI C3037; confirmed ICD10 G93.32; confirmed ORPHANET 1983; confirmed UMLS C0015674; confirmed MESH D015673; flagged ICD10 780.71
2026-08-12 01:11 | KrishnaTO | Cross-reference review: confirmed SNOMED 52702003; confirmed OMOP 432738; confirmed DOID 8544; confirmed MONDO 0005404; confirmed NCI C3037; confirmed ICD10 G93.32; confirmed ORPHANET 1983; confirmed UMLS C0015674; confirmed MESH D015673; flagged ICD10 780.71
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: no term in OMIM
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: no term in OMIM
@@ -6965,7 +6927,7 @@ The cause of this syndrome is unknown, however, researchers believe that it may
2026-08-12 01:11 | KrishnaTO | Cross-reference review: confirmed SNOMED 128209004; confirmed OMOP 381009; confirmed DOID 5213; confirmed MONDO 0006702; confirmed NCI C84636; confirmed ICD10 G61.81; confirmed ORPHANET 2932; confirmed UMLS C0393819; confirmed MESH D020277; flagged SNOMED 230564004; flagged OMOP 4048024; flagged ICD10 357.81
128209004
381009
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: no term in OMIM
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: no term in OMIM
@@ -7088,7 +7050,7 @@ Currently, the cause of interstitial cystitis is unknown. There are two main the
2026-08-03 18:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 38731000087104; confirmed OMOP 1450471; confirmed DOID 1678; confirmed MONDO 0018301; confirmed NCI C27189; confirmed ICD10 N30.1; confirmed ORPHANET 37202; confirmed UMLS C0600040; confirmed MESH D018856
2026-08-03 18:15 | KrishnaTO | Cross-reference review: confirmed SNOMED 38731000087104; confirmed OMOP 1450471; confirmed DOID 1678; confirmed MONDO 0018301; confirmed NCI C27189; confirmed ICD10 N30.1; confirmed ORPHANET 37202; confirmed UMLS C0600040; confirmed MESH D018856
2026-08-12 01:11 | KrishnaTO | Cross-reference review: confirmed SNOMED 38731000087104; confirmed OMOP 1450471; confirmed DOID 1678; confirmed MONDO 0018301; confirmed NCI C27189; confirmed ICD10 N30.1; confirmed ORPHANET 37202; confirmed UMLS C0600040; confirmed MESH D018856
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: no term in OMIM
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: no term in OMIM
@@ -7230,17 +7192,7 @@ However, in some people, the Lyme disease triggers symptoms similar to rheumatoi
2026-08-03 18:00 | KrishnaTO | Cross-reference review: flagged DOID 11729; flagged ICD10 088.81, A69.2; flagged SNOMED 1269516003
2026-08-03 18:15 | KrishnaTO | Cross-reference review: flagged DOID 11729; flagged ICD10 088.81, A69.2; flagged SNOMED 1269516003
2026-08-12 01:11 | KrishnaTO | Cross-reference review: flagged DOID 11729; flagged ICD10 088.81, A69.2; flagged SNOMED 1269516003
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: confirmed MONDO 0700280; confirmed NCI C119039; confirmed UMLS C3890422; confirmed MESH D000077342; no term in ORPHANET; no term in DOID; no term in SNOMED; no term in ICD10; no term in OMIM
- Syndromes, Post-Lyme Disease
- PTLDS
- disorder due to consequences of Lyme disease
- post-Lyme disease
- Post-Lyme Disease Syndromes
- Syndrome, Post-Lyme Disease
- Lyme Disease, Chronic
- post-Lyme disease syndrome
- post-treatment Lyme disease syndrome
- 2026-08-18 00:06 | KrishnaTO | Enrichment from confirmed cross-references: +9 synonym(s)
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: confirmed MONDO 0700280; confirmed NCI C119039; confirmed UMLS C3890422; confirmed MESH D000077342; no term in ORPHANET; no term in DOID; no term in SNOMED; no term in ICD10; no term in OMIM
@@ -7453,7 +7405,7 @@ Chronic non-bacterial osteomyelitis (CNO) is a rare auto-inflammatory bone disor
2026-08-03 18:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 1204420006; confirmed OMOP 37163124; confirmed DOID 0060645; confirmed MONDO 0009813; confirmed NCI C119042; confirmed ICD10 M86.3; confirmed ORPHANET 324964; confirmed UMLS C0410422; confirmed MESH C535456; flagged OMIM 609628
2026-08-03 18:15 | KrishnaTO | Cross-reference review: confirmed SNOMED 1204420006; confirmed OMOP 37163124; confirmed DOID 0060645; confirmed MONDO 0009813; confirmed NCI C119042; confirmed ICD10 M86.3; confirmed ORPHANET 324964; confirmed UMLS C0410422; confirmed MESH C535456; flagged OMIM 609628
2026-08-12 01:11 | KrishnaTO | Cross-reference review: confirmed SNOMED 1204420006; confirmed OMOP 37163124; confirmed DOID 0060645; confirmed MONDO 0009813; confirmed NCI C119042; confirmed ICD10 M86.3; confirmed ORPHANET 324964; confirmed UMLS C0410422; confirmed MESH C535456; flagged OMIM 609628
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: no term in OMIM
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: no term in OMIM
@@ -7685,7 +7637,7 @@ More study is needed.
2026-08-03 18:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 1119304009; confirmed OMOP 600589; confirmed DOID 0080848; confirmed MONDO 0100233; confirmed NCI C179263; confirmed UMLS C5433293; confirmed MESH D000094024
2026-08-03 18:15 | KrishnaTO | Cross-reference review: confirmed SNOMED 1119304009; confirmed OMOP 600589; confirmed DOID 0080848; confirmed MONDO 0100233; confirmed NCI C179263; confirmed UMLS C5433293; confirmed MESH D000094024
2026-08-12 01:11 | KrishnaTO | Cross-reference review: confirmed SNOMED 1119304009; confirmed OMOP 600589; confirmed DOID 0080848; confirmed MONDO 0100233; confirmed NCI C179263; confirmed UMLS C5433293; confirmed MESH D000094024
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: no term in ORPHANET; no term in OMIM
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: no term in ORPHANET; no term in OMIM
@@ -7798,10 +7750,7 @@ More study is needed.
2026-08-03 18:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 405810005; confirmed OMOP 4233620; confirmed ICD10 H16.32; confirmed ORPHANET 1467; confirmed MESH D055952; flagged ICD10 370.52; flagged UMLS C0155089
2026-08-03 18:15 | KrishnaTO | Cross-reference review: confirmed SNOMED 405810005; confirmed OMOP 4233620; confirmed ICD10 H16.32; confirmed ORPHANET 1467; confirmed MESH D055952; flagged ICD10 370.52; flagged UMLS C0155089
2026-08-12 01:11 | KrishnaTO | Cross-reference review: confirmed SNOMED 405810005; confirmed OMOP 4233620; confirmed ICD10 H16.32; confirmed ORPHANET 1467; confirmed MESH D055952; flagged ICD10 370.52; flagged UMLS C0155089
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: confirmed DOID 0060216; confirmed MONDO 0015453; confirmed UMLS C0271270; no term in NCI; no term in OMIM
- Cogan syndrome
- diffuse interstitual keratitis
- 2026-08-18 00:06 | KrishnaTO | Enrichment from confirmed cross-references: +2 synonym(s)
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: confirmed DOID 0060216; confirmed MONDO 0015453; confirmed UMLS C0271270; no term in NCI; no term in OMIM
@@ -7973,29 +7922,7 @@ More study is needed.
2026-08-12 01:11 | KrishnaTO | Cross-reference review: confirmed SNOMED 398937006; confirmed OMOP 4160887; confirmed MONDO 0018922; confirmed NCI C208228; confirmed ICD10 D59.12; confirmed ORPHANET 56425; confirmed UMLS C0175816; flagged SNOMED 127055007; flagged OMOP 4131128
398937006
4160887
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: confirmed MESH D000744; no term in OMIM; no term in DOID
- Anaemia, Autoimmune Haemolytic
- Autoimmune Haemolytic Anaemias
- AIHA
- Autoimmune haemolytic anaemia
- Autoimmune Hemolytic Anemias
- autoimmune haemolytic anemia
- autoimmune hemolytic anaemia
- autoimmune hemolytic anemia
- Anemia, Hemolytic, Autoimmune
- AHA
- Anemia, Hemolytic, Acquired Autoimmune
- Hemolytic Anemia, Autoimmune
- Haemolytic Anaemia, Autoimmune
- Anemia, Autoimmune Hemolytic
- Evans syndrome - subtype of Cold agglutinin disease (MONDO:0016030)
- neonatal autoimmune hemolytic anemia - subtype of Cold agglutinin disease (MONDO:0018358)
- drug-induced autoimmune hemolytic anemia - subtype of Cold agglutinin disease (MONDO:0019535)
- giant cell hepatitis with autoimmune hemolytic anemia - subtype of Cold agglutinin disease (MONDO:1060166)
- autoimmune hemolytic anemia, warm type - subtype of Cold agglutinin disease (MONDO:0019532)
- autoimmune hemolytic anemia, cold type - subtype of Cold agglutinin disease (MONDO:0016450)
- mixed-type autoimmune hemolytic anemia - subtype of Cold agglutinin disease (MONDO:0019534)
- 2026-08-18 00:06 | KrishnaTO | Enrichment from confirmed cross-references: +14 synonym(s), +7 clinical subtype(s)
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: confirmed MESH D000744; no term in OMIM; no term in DOID
@@ -8129,10 +8056,7 @@ More study is needed.
2026-08-03 18:00 | KrishnaTO | Cross-reference review: confirmed SNOMED 1197477000; confirmed OMOP 37162777; confirmed DOID 0081151; confirmed MONDO 0013863; confirmed ORPHANET 445018; confirmed OMIM 614700; confirmed UMLS C3553512
2026-08-03 18:15 | KrishnaTO | Cross-reference review: confirmed SNOMED 1197477000; confirmed OMOP 37162777; confirmed DOID 0081151; confirmed MONDO 0013863; confirmed ORPHANET 445018; confirmed OMIM 614700; confirmed UMLS C3553512
2026-08-12 01:11 | KrishnaTO | Cross-reference review: confirmed SNOMED 1197477000; confirmed OMOP 37162777; confirmed DOID 0081151; confirmed MONDO 0013863; confirmed ORPHANET 445018; confirmed OMIM 614700; confirmed UMLS C3553512
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: confirmed NCI C176809; no term in ICD10; no term in MESH
- Immunodeficiency, Common Variable, 8, with Autoimmunity
- CVID8
- 2026-08-18 00:06 | KrishnaTO | Enrichment from confirmed cross-references: +2 synonym(s)
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: confirmed NCI C176809; no term in ICD10; no term in MESH
@@ -8196,11 +8120,7 @@ More study is needed.
2026-08-12 01:11 | KrishnaTO | Cross-reference review: confirmed SNOMED 128200000; confirmed OMOP 4134577; confirmed DOID 3223; confirmed MONDO 0019369; confirmed NCI C206547; confirmed ORPHANET 83452; confirmed UMLS C0458219; confirmed MESH D020918; flagged SNOMED 408751001, 734947007; flagged OMOP 42536233, 4256912
128200000
4134577
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: confirmed OMIM 604335; confirmed ICD10 M89.0
- algoneurodystrophy
- complex regional pain syndrome type 2 - subtype of Complex regional pain syndrome (MONDO:0020572)
- complex regional pain syndrome type 1 - subtype of Complex regional pain syndrome (MONDO:0011441)
- 2026-08-18 00:06 | KrishnaTO | Enrichment from confirmed cross-references: +1 synonym(s), +2 clinical subtype(s)
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: confirmed OMIM 604335; confirmed ICD10 M89.0
@@ -8371,24 +8291,7 @@ Both UC and CD are caused by an autoimmune response that reflects the involvemen
C2965
2026-08-12 01:01 | user | Edited: nci
2026-08-12 01:11 | KrishnaTO | Cross-reference review: confirmed SNOMED 34000006; confirmed MONDO 0005011; confirmed DOID 8778; flagged ICD10 555.1
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: confirmed ICD10 K50; confirmed NCI C2965; confirmed OMOP 201606; confirmed ORPHANET 206; confirmed MESH D003424
- paediatric Crohn's disease
- Crohn disease
- NON RARE IN EUROPE: Crohn disease
- pediatric Crohn's disease
- Inflammatory Bowel Disease 1
- Crohn's Enteritis
- regional enteritis
- Crohn's disease of large bowel
- Crohns Disease
- perianal Crohn disease - subtype of Crohn's disease (MONDO:0005537)
- Crohn Disease of Rectum - subtype of Crohn's disease (NCIT:C219892)
- Crohn disease of the esophagus - subtype of Crohn's disease (MONDO:0022901)
- Crohn Colitis - subtype of Crohn's disease (NCIT:C35211)
- small bowel Crohn disease - subtype of Crohn's disease (MONDO:0005539)
- oral Crohn disease - subtype of Crohn's disease (MONDO:0005535)
- Crohn Disease of Small Intestine - subtype of Crohn's disease (NCIT:C35210)
- 2026-08-18 00:06 | KrishnaTO | Enrichment from confirmed cross-references: +9 synonym(s), +7 clinical subtype(s)
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: confirmed ICD10 K50; confirmed NCI C2965; confirmed OMOP 201606; confirmed ORPHANET 206; confirmed MESH D003424
@@ -8507,28 +8410,7 @@ Both UC and CD are caused by an autoimmune response that reflects the involvemen
2024-09
COP
2026-06-15 10:37 | Importer | Imported from ARI core reports
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: confirmed SNOMED 719218000; confirmed OMOP 36714118; confirmed DOID 2797; confirmed MONDO 0015264; confirmed ORPHANET 1302; no term in OMIM
- noninfectious pneumonia
- Idiopathic fibrosing alveolitis
- bronchiolitis obliterans organizing pneumonia
- Organizing Pneumonia
- cryptogenic organizing pneumonitis
- Diffuse idiopathic pulmonary fibrosis
- idiopathic interstitial pneumonitis
- COP
- BOOP
- organising pneumonia
- respiratory bronchiolitis-interstitial lung disease syndrome - subtype of Cryptogenic organizing pneumonia (MONDO:0019204)
- idiopathic pulmonary fibrosis - subtype of Cryptogenic organizing pneumonia (MONDO:0800504)
- combined pulmonary fibrosis-emphysema syndrome - subtype of Cryptogenic organizing pneumonia (MONDO:0017591)
- desquamative interstitial pneumonia - subtype of Cryptogenic organizing pneumonia (DOID:0050158)
- nonspecific interstitial pneumonia - subtype of Cryptogenic organizing pneumonia (DOID:2801)
- follicular bronchiolits - subtype of Cryptogenic organizing pneumonia (MONDO:0800114)
- non-specific interstitial pneumonia - subtype of Cryptogenic organizing pneumonia (MONDO:0019622)
- acute interstitial pneumonia - subtype of Cryptogenic organizing pneumonia (DOID:2800)
- idiopathic pleuroparenchymal fibroelastosis - subtype of Cryptogenic organizing pneumonia (MONDO:0044633)
- lymphoid interstitial pneumonia - subtype of Cryptogenic organizing pneumonia (DOID:0050159)
- 2026-08-18 00:06 | KrishnaTO | Enrichment from confirmed cross-references: +10 synonym(s), +10 clinical subtype(s)
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: confirmed SNOMED 719218000; confirmed OMOP 36714118; confirmed DOID 2797; confirmed MONDO 0015264; confirmed ORPHANET 1302; no term in OMIM
@@ -8614,17 +8496,7 @@ Both UC and CD are caused by an autoimmune response that reflects the involvemen
2026-06-15 10:37 | Importer | Imported from ARI core reports
7119001
4324123
- 2026-08-18 00:06 | KrishnaTO | Cross-reference review: confirmed DOID 0050169; confirmed MONDO 0005282; confirmed NCI C26819; confirmed UMLS C0024137; confirmed MESH D008178; no term in OMIM
- Lupus Erythematosus, Cutaneous
- subacute cutaneous lupus erythematosus - subtype of Cutaneous lupus erythematosus (MONDO:0015573)
- chronic cutaneous lupus erythematosus - subtype of Cutaneous lupus erythematosus (MONDO:0015574)
- Systemic Lupus Erythematosus Rash - subtype of Cutaneous lupus erythematosus (NCIT:C27171)
- bullous systemic lupus erythematosus - subtype of Cutaneous lupus erythematosus (MONDO:0044113)
- Lupus Erythematosus Tumidus - subtype of Cutaneous lupus erythematosus (NCIT:C117112)
- Rowell syndrome - subtype of Cutaneous lupus erythematosus (MONDO:0041186)
- Drug Induced Cutaneous Lupus Erythematosus - subtype of Cutaneous lupus erythematosus (NCIT:C112203)
- Chilblain lupus - subtype of Cutaneous lupus erythematosus (DOID:0060386)
- 2026-08-18 00:06 | KrishnaTO | Enrichment from confirmed cross-references: +1 synonym(s), +8 clinical subtype(s)
+ 2026-08-20 16:32 | KrishnaTO | Cross-reference review: confirmed DOID 0050169; confirmed MONDO 0005282; confirmed NCI C26819; confirmed UMLS C0024137; confirmed MESH D008178; no term in OMIM