@@ -29382,8 +29382,7 @@ SubClassOf(obo:DOID_0060061 obo:DOID_0050749)
2938229382
2938329383# Class: obo:DOID_0060062 (autosomal dominant tubulointerstitial kidney disease)
2938429384
29385- AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/21060763") obo:IAO_0000115 obo:DOID_0060062 "A kidney disease that is characterized by hyperuricemia with renal uric acid under-excretion, gout and chronic kidney disease.")
29386- AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060062 "MIM:614227")
29385+ AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/books/NBK1356/") obo:IAO_0000115 obo:DOID_0060062 "A kidney disease that is characterized by normal urinalysis and slowly progressive chronic kidney disease, usually first noted in the teen years and progressing to end-stage renal disease between the third and seventh decades.")
2938729386AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060062 "ORDO:34149")
2938829387AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0060062 "HNFJ")
2938929388AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0060062 "MCKD")
@@ -29397,7 +29396,7 @@ AnnotationAssertion(rdfs:label obo:DOID_0060062 "autosomal dominant tubulointers
2939729396AnnotationAssertion(skos:narrowMatch obo:DOID_0060062 "MIM:614227")
2939829397SubClassOf(obo:DOID_0060062 obo:DOID_557)
2939929398SubClassOf(obo:DOID_0060062 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))
29400- SubClassOf(obo:DOID_0060062 ObjectSomeValuesFrom(obo:RO_0002488 obo:HP_0011462 ))
29399+ SubClassOf(obo:DOID_0060062 ObjectSomeValuesFrom(obo:RO_0002488 obo:HP_0003581 ))
2940129400
2940229401# Class: obo:DOID_0060063 (sideroblastic anemia 1)
2940329402
@@ -43811,6 +43810,7 @@ AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061118 "disease_ontology"
4381143810AnnotationAssertion(oboInOwl:id obo:DOID_0061118 "DOID:0061118")
4381243811AnnotationAssertion(rdfs:label obo:DOID_0061118 "autosomal dominant tubulointerstitial kidney disease 2")
4381343812SubClassOf(obo:DOID_0061118 obo:DOID_0060062)
43813+ SubClassOf(obo:DOID_0061118 ObjectSomeValuesFrom(obo:RO_0002488 obo:HP_0003581))
4381443814
4381543815# Class: obo:DOID_0061119 (autosomal dominant tubulointerstitial kidney disease 4)
4381643816
@@ -43850,6 +43850,7 @@ AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061121 "disease_ontology"
4385043850AnnotationAssertion(oboInOwl:id obo:DOID_0061121 "DOID:0061121")
4385143851AnnotationAssertion(rdfs:label obo:DOID_0061121 "autosomal dominant tubulointerstitial kidney disease 6")
4385243852SubClassOf(obo:DOID_0061121 obo:DOID_0060062)
43853+ SubClassOf(obo:DOID_0061121 ObjectSomeValuesFrom(obo:RO_0002488 obo:HP_0003581))
4385343854
4385443855# Class: obo:DOID_0061122 (autosomal dominant tubulointerstitial kidney disease 1)
4385543856
@@ -43863,6 +43864,7 @@ AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0061122 "disease_ontology"
4386343864AnnotationAssertion(oboInOwl:id obo:DOID_0061122 "DOID:0061122")
4386443865AnnotationAssertion(rdfs:label obo:DOID_0061122 "autosomal dominant tubulointerstitial kidney disease 1")
4386543866SubClassOf(obo:DOID_0061122 obo:DOID_0060062)
43867+ SubClassOf(obo:DOID_0061122 ObjectSomeValuesFrom(obo:RO_0002488 obo:HP_0003581))
4386643868
4386743869# Class: obo:DOID_0070000 (3-methylglutaconic aciduria type 8)
4386843870
@@ -54019,9 +54021,9 @@ AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080122 "Alpers progressiv
5401954021AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080122 "Alpers syndrome")
5402054022AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080122 "Alpers' disease or gray-matter degeneration")
5402154023AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080122 "Diffuse Cerebral Sclerosis of Schilder")
54024+ AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080122 "Polg disease")
5402254025AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080122 "mitochondrial DNA depletion syndrome 4a")
5402354026AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080122 "progressive sclerosing poliodystrophy")
54024- AnnotationAssertion(oboInOwl:hasExactSynonym obo:DOID_0080122 "Polg disease")
5402554027AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0080122 "disease_ontology")
5402654028AnnotationAssertion(oboInOwl:id obo:DOID_0080122 "DOID:0080122")
5402754029AnnotationAssertion(oboInOwl:inSubset obo:DOID_0080122 doid:DO_rare_slim)
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