| manager |
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| language |
- |
| license |
- |
| created at |
2021-12-20 14:06:07 UTC |
| updated at |
2021-12-22 07:06:57 UTC |
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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 }
}
}
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110,360 entries
|
There is 0 pattern entry.
|
mannosyltransferase 6 deficiency
|
0010998 |
|
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ALG3-CDG
|
0010998 |
|
|
CDG-Id
|
0010998 |
|
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CDG1D
|
0010998 |
|
|
CDGId
|
0010998 |
|
|
ALG3-CDG (CDG-Id)
|
0010998 |
|
|
CDG 1D
|
0010998 |
|
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CDG Id
|
0010998 |
|
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CDGS4 (formerly)
|
0010998 |
|
|
carbohydrate-deficient glycoprotein syndrome type IV (formerly)
|
0010998 |
|
|
carbohydrate deficient glycoprotein syndrome type Id
|
0010998 |
|
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congenital disorder of glycosylation type 1d
|
0010998 |
|
|
congenital disorder of glycosylation type Id
|
0010998 |
|
|
congenital disorder of glycosylation, type Id
|
0010998 |
|
|
Cdgs, type IV
|
0010998 |
|
