| manager |
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| language |
- |
| license |
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| 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
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There is 0 pattern entry.
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ARCL3A
|
0009053 |
|
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P5CS deficiency
|
0009053 |
|
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ALDH18A1-related de Barsy syndrome
|
0009053 |
|
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neurocutaneous syndrome, Bicknell type
|
0009053 |
|
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cutis laxa, autosomal recessive, type 3A
|
0009053 |
|
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cutis laxa, autosomal recessive, type IIIA
|
0009053 |
|
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cutis laxa, corneal clouding, and intellectual disability
|
0009053 |
|
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cutis laxa, corneal clouding, and mental retardation
|
0009053 |
|
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autosomal recessive cutis laxa type IIIA
|
0009053 |
|
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progeroid syndrome of De Barsy
|
0009053 |
|
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De Barsy syndrome A
|
0009053 |
|
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De Barsy syndrome a
|
0009053 |
|
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Delta-1-pyrroline 5-carboxylate synthetase deficiency
|
0009053 |
|
