| manager |
|
| language |
- |
| license |
- |
| created at |
2021-12-20 14:06:07 UTC |
| updated at |
2021-12-22 07:06:57 UTC |
|
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.
|
ADT1P
|
0008289 |
|
|
BSVD
|
0008289 |
|
|
BSVD1
|
0008289 |
|
|
POREN1
|
0008289 |
|
|
T1P
|
0008289 |
|
|
COL4A1 porencephaly
|
0008289 |
|
|
infantile hemiparesis
|
0008289 |
|
|
porencephaly 1
|
0008289 |
|
|
porencephaly type 1
|
0008289 |
|
|
porencephaly, type 1, autosomal dominant
|
0008289 |
|
|
COL4A1-related retinal arteriolar tortuosity-infantile hemiparesis-autosomal dominant leukoencephalopathy syndrome
|
0008289 |
|
|
leukoencephalopathy with axenfeld-rieger anomaly
|
0008289 |
|
|
COL4A1-related familial vascular leukoencephalopathy
|
0008289 |
|
|
brain small vessel disease 1 with or without ocular anomalies
|
0008289 |
|
|
brain small vessel disease with Axenfeld-Riegar anomaly
|
0008289 |
|
