MONDO_label_synonym Find_IDs Find_Terms Annotation
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created at 2021-12-20 14:06:07 UTC
updated at 2021-12-22 07:06:57 UTC
PREFIX owl: <http://www.w3.org/2002/07/owl#>
PREFIX rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#>
PREFIX rdfs: <http://www.w3.org/2000/01/rdf-schema#>
PREFIX obo: <http://www.geneontology.org/formats/oboInOwl#>
SELECT DISTINCT ?label (SUBSTR(str(?sub),38) AS ?id) WHERE {
?sub rdfs:subClassOf+ <http://purl.obolibrary.org/obo/MONDO_0000001> ;
rdf:type owl:Class .
{ { ?sub rdfs:label ?label }
UNION { ?sub obo:hasBroadSynonym ?label }
UNION { ?sub obo:hasExactSynonym ?label }
UNION { ?sub obo:hasRelatedSynonym ?label }
}
}
110,360 entries
Label
Id
congenital ADAMTS-13 deficiency 0010122
congenital ADAMTS13 deficiency 0010122
TTP 0010122
USS 0010122
Schulman-Upshaw syndrome 0010122
TTP, congenital 0010122
Upshaw-Schulman syndrome 0010122
congenital TTP 0010122
familial TTP 0010122
Microangiopathic hemolytic Anemia 0010122
Microangiopathic hemolytic Anemia, congenital 0010122
Upshaw Factor, deficiency of 0010122
thrombotic microangiopathy, familial 0010122
thrombotic thrombocytopenic purpura, congenital 0010122
thrombotic thrombocytopenic purpura, familial 0010122