| 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
|
There is 0 pattern entry.
|
AHD
|
0008758 |
|
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AHS
|
0008758 |
|
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MTDPS4A
|
0008758 |
|
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PNDC
|
0008758 |
|
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Alper syndrome
|
0008758 |
|
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Alper's syndrome
|
0008758 |
|
|
Alpers disease
|
0008758 |
|
|
Alpers syndrome
|
0008758 |
|
|
Alpers-Huttenlocher syndrome
|
0008758 |
|
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infantile poliodystrophy
|
0008758 |
|
|
Alpers diffuse Degeneration of cerebral Gray matter with hepatic cirrhosis
|
0008758 |
|
|
diffuse cerebral degeneration in infancy
|
0008758 |
|
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progressive neuronal degeneration of childhood with liver disease
|
0008758 |
|
|
mitochondrial DNA depletion syndrome 4A
|
0008758 |
|
|
mitochondrial DNA depletion syndrome 4A (Alpers type)
|
0008758 |
|
