| manager |
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| language |
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| 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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Alpha-sarcoglycanopathy
|
0011968 |
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DMDA2
|
0011968 |
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LGMD2D
|
0011968 |
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Adhalinopathy, primary
|
0011968 |
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primary adhalinopathy
|
0011968 |
|
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limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency
|
0011968 |
|
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limb-girdle muscular dystrophy type 2D
|
0011968 |
|
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limb-girdle muscular dystrophy, type 2D
|
0011968 |
|
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autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCA
|
0011968 |
|
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autosomal recessive limb-girdle muscular dystrophy type 2D
|
0011968 |
|
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muscular dystrophy limb-girdle with alpha-sarcoglycan
|
0011968 |
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muscular dystrophy, limb-girdle, type 2D
|
0011968 |
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SGCA autosomal recessive limb-girdle muscular dystrophy
|
0011968 |
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Duchenne-like autosomal recessive muscular dystrophy type 2
|
0011968 |
|
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Duchenne-like autosomal recessive muscular dystrophy, type 2
|
0011968 |
|
