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
retinal arteriolar tortuosity, infantile hemiparesis, and leukoencephalopathy, autosomal dominant 0008289
brain small vessel disease 1 with or without ocular anomalies 0008289
brain small vessel disease with Axenfeld-Riegar anomaly 0008289
brain small vessel disease with axenfeld-rieger anomaly 0008289
brain small vessel disease with hemorrhage 0008289
brain small vessel disease with or without ocular anomalies 0008289
hemiplegia, infantile, with porencephaly 0008289
hemiplegia, infantile, with porencephaly porencephaly, type 1 0008289
autosomal dominant retinal arteriolar tortuosity, infantile hemiparesis, and leukencephalopathy 0008289