| 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 }
}
}
|
110,360 entries
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There is 0 pattern entry.
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AOA1
|
0008842 |
|
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EAOH
|
0008842 |
|
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EOCA-HA
|
0008842 |
|
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ataxia-telangiectasia-like syndrome
|
0008842 |
|
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ataxia-oculomotor apraxia 1
|
0008842 |
|
|
oculomotor apraxia or related oculomotor disease caused by mutation in APTX
|
0008842 |
|
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APTX oculomotor apraxia or related oculomotor disease
|
0008842 |
|
|
ataxia with oculomotor apraxia type 1
|
0008842 |
|
|
early-onset cerebellar ataxia with hypoalbuminemia
|
0008842 |
|
|
cerebellar ataxia, early-onset, with hypoalbuminemia
|
0008842 |
|
|
ataxia-oculomotor apraxia syndrome
|
0008842 |
|
|
ataxia-oculomotor apraxia type 1
|
0008842 |
|
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ataxia, adult-onset, with oculomotor apraxia
|
0008842 |
|
|
ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
|
0008842 |
|
|
early-onset ataxia with oculomotor apraxia and hypoalbuminemia
|
0008842 |
|
