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Update "Henoch-Schoenlein purpura" to "IgA vasculitis"
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‎src/ontology/doid-edit.owl‎

Lines changed: 22 additions & 7 deletions
Original file line numberDiff line numberDiff line change
@@ -27597,7 +27597,7 @@ SubClassOf(obo:DOID_0050956 obo:DOID_1441)
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# Class: obo:DOID_0050957 (spinocerebellar ataxia type 4)
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AnnotationAssertion(Annotation(dc:type obo:ECO_0007637) Annotation(oboInOwl:hasDbXref "url:https://rarediseases.info.nih.gov/diseases/9970/spinocerebellar-ataxia-4") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/38035881/") obo:IAO_0000115 obo:DOID_0050957 "An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and peripheral neuropathy that has_material_basis_in heterozygous trinucleotide repeat expansion (GGCn) in the ZFHX3 gene on chromosome 16q22.")
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AnnotationAssertion(Annotation(dc:type obo:ECO_0007637) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/38035881/") Annotation(oboInOwl:hasDbXref "url:https://rarediseases.info.nih.gov/diseases/9970/spinocerebellar-ataxia-4") obo:IAO_0000115 obo:DOID_0050957 "An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and peripheral neuropathy that has_material_basis_in heterozygous trinucleotide repeat expansion (GGCn) in the ZFHX3 gene on chromosome 16q22.")
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AnnotationAssertion(oboInOwl:created_by obo:DOID_0050957 "lschriml")
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AnnotationAssertion(oboInOwl:creation_date obo:DOID_0050957 "2015-10-05T16:07:27Z")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0050957 "GARD:9970")
@@ -31694,11 +31694,11 @@ AnnotationAssertion(oboInOwl:created_by obo:DOID_0060234 "emitraka")
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AnnotationAssertion(oboInOwl:creation_date obo:DOID_0060234 "2015-01-23T16:06:03Z")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060234 "GARD:6003")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060234 "MESH:C563187")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060234 "MIM:PS201000")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060234 "NCI:C98873")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060234 "ORDO:65759")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060234 "SNOMEDCT_US_2023_03_01:403767009")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060234 "UMLS_CUI:C1275078")
31701-
AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060234 "MIM:PS201000")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0060234 "acrocephalopolysyndactyly type II")
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AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0060234 "disease_ontology")
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AnnotationAssertion(oboInOwl:id obo:DOID_0060234 "DOID:0060234")
@@ -113006,28 +113006,43 @@ AnnotationAssertion(oboInOwl:inSubset obo:DOID_11121 doid:NCIthesaurus)
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AnnotationAssertion(rdfs:label obo:DOID_11121 "pulpitis")
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SubClassOf(obo:DOID_11121 obo:DOID_5330)
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# Class: obo:DOID_11123 (Henoch-Schoenlein purpura)
113009+
# Class: obo:DOID_11123 (IgA vasculitis)
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AnnotationAssertion(Annotation(dc:type obo:ECO_0007637) Annotation(oboInOwl:hasDbXref "url:https://rarediseases.info.nih.gov/diseases/8204/henoch-schonlein-purpura") obo:IAO_0000115 obo:DOID_11123 "A hypersensitivity vasculitis that is characterized by purpura (purplish plaques), arthralgia, gastrointestinal upset, and/or glomerulonephritis, and may be related to increased immune response following an infection.")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_11123 "GARD:8204")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_11123 "ICD10CM:D69.0")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_11123 "ICD9CM:287.0")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_11123 "MESH:D011695")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_11123 "NCI:C34963")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_11123 "ORDO:761")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_11123 "SNOMEDCT_US_2023_03_01:191306005")
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AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_11123 "UMLS_CUI:C0034152")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Allergic purpura")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Autoimmune purpura")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Henoch-Sch?nlein purpura")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Henoch-Sch@nlein purpura")
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AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_11123 "HSP")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Henoch Schoenlein purpura")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Henoch Scholein purpura")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Henoch Schonlein purpura")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Henoch Schönlein purpura")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Henoch-Schoenlein purpura")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Henoch-Scholein purpura")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Henoch-Schonlein Purpura")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Henoch-Schonlein purpura")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Henoch-Schönlein purpura")
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AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_11123 "IgAV")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "Purpura, autoimmune")
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AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_11123 "immunoglobulin A vasculitis")
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AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_11123 "disease_ontology")
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AnnotationAssertion(oboInOwl:id obo:DOID_11123 "DOID:11123")
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AnnotationAssertion(oboInOwl:inSubset obo:DOID_11123 doid:DO_rare_slim)
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AnnotationAssertion(oboInOwl:inSubset obo:DOID_11123 doid:NCIthesaurus)
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AnnotationAssertion(rdfs:label obo:DOID_11123 "Henoch-Schoenlein purpura")
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AnnotationAssertion(rdfs:label obo:DOID_11123 "IgA vasculitis")
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AnnotationAssertion(skos:exactMatch obo:DOID_11123 "GARD:8204")
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AnnotationAssertion(skos:exactMatch obo:DOID_11123 "ICD10CM:D69.0")
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AnnotationAssertion(skos:exactMatch obo:DOID_11123 "ICD9CM:287.0")
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AnnotationAssertion(skos:exactMatch obo:DOID_11123 "MESH:D011695")
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AnnotationAssertion(skos:exactMatch obo:DOID_11123 "NCI:C34963")
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AnnotationAssertion(skos:exactMatch obo:DOID_11123 "ORDO:761")
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AnnotationAssertion(skos:exactMatch obo:DOID_11123 "UMLS_CUI:C0034152")
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SubClassOf(obo:DOID_11123 obo:DOID_9809)
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# Class: obo:DOID_11125 (qualitative platelet defect)

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