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Dictionary name: qald-diseasome

Creator:

jdkim@dbcls.rois.ac.jp

Description:

Diseasome dataset as included in QALD

Entry nameIDLabel
1-30 / 8149 show all
17,20-lyase deficiencyhttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/0
17,20-lyase deficiency, isolated, 202110http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1284
17-alpha-hydroxylase/17,20-lyase deficiency, 202110http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1285
2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiencyhttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1
2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, 300438http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1286
2-methylbutyrylglycinuriahttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1287
2-methylbutyrylglycinuriahttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/2
3-beta-hydroxysteroid dehydrogenase, type II, deficiencyhttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1288
3-beta-hydroxysteroid dehydrogenase, type II, deficiencyhttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/3
3-hydroxyacyl-CoA dehydrogenase deficiencyhttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/4
3-hydroxyacyl-CoA dehydrogenase deficiency, 609609http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1289
3-Methylcrotonyl-CoA carboxylase 1 deficiency, 210200http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1290
3-Methylcrotonyl-CoA carboxylase 2 deficiency, 210210http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1291
3-Methylcrotonyl-CoA carboxylase deficiencyhttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/5
3-methylglutaconicaciduriahttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/7
3-methylglutaconic aciduriahttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/6
3-methylglutaconic aciduria, type I, 250950http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1292
3-methylglutaconicaciduria, type III, 258501http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1293
3-M syndromehttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/8
3-M syndrome, 273750http://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1294
6-mercaptopurine sensitivityhttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/1295
6-mercaptopurine sensitivityhttp://www4.wiwiss.fu-berlin.de/diseasome/resource/diseases/9
A15http://www4.wiwiss.fu-berlin.de/diseasome/resource/genes/A15
A2Mhttp://www4.wiwiss.fu-berlin.de/diseasome/resource/genes/A2M
A4GALThttp://www4.wiwiss.fu-berlin.de/diseasome/resource/genes/A4GALT
AAAhttp://www4.wiwiss.fu-berlin.de/diseasome/resource/genes/AAA
AAAShttp://www4.wiwiss.fu-berlin.de/diseasome/resource/genes/AAAS
AAC2http://www4.wiwiss.fu-berlin.de/diseasome/resource/genes/AAC2
AACThttp://www4.wiwiss.fu-berlin.de/diseasome/resource/genes/AACT
AANAThttp://www4.wiwiss.fu-berlin.de/diseasome/resource/genes/AANAT

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