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Dictionary name: GDGDB_DISEASE_NAME

Creator:

t.shikanai@aist.go.jp

Description:

Genetic Glyco-Diseases Ontology (GGDonto) and Glyco-Disease Genes DataBase (GDGDB)

Entry nameIDLabel
1-30 / 356 show all
ACG1Bhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00396
ACHONDROGENESIS, FRACCARO TYPEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00396
ADDUCTED THUMB, CLUBFOOT, AND PROGRESSIVE JOINT AND SKIN LAXITY SYNDROMEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00634
ADDUCTED THUMB-CLUBFOOT SYNDROMEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00634
AGA DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00005
AGUhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00005
ALKURAYA SYNDROMEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00358
ALPHA-MANNOSIDASE B DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00008
ALPHA-MANNOSIDOSIShttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00008
Anemia, Dyserythropoietic, Congenital Type 2http://acgg.asia/db/diseases/gdgdb?con_ui=CON00373
AO2http://acgg.asia/db/diseases/gdgdb?con_ui=CON00397
AOIIhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00397
ARCL2http://acgg.asia/db/diseases/gdgdb?con_ui=CON00371
ARCL2Ahttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00371
ARTHROGRYPOSIS, DISTAL, WITH PECULIAR FACIES AND HYDRONEPHROSIShttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00634
ASPARTYLGLUCOSAMINIDASE DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00005
ASPARTYLGLYCOSAMINURIAhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00005
ATCShttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00634
Atelosteogenesis de la Chapelle typehttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00397
BETA-MANNOSIDASE DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00011
BETA-MANNOSIDOSIShttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00011
BRKS2http://acgg.asia/db/diseases/gdgdb?con_ui=CON00408
B VARIANT GM2-GANGLIOSIDOSIShttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00055
C1型Niemann-Pick病@jahttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00089
C1型ニーマン・ピック病@jahttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00089
CALCINOSIS, TUMORAL, WITH HYPERPHOSPHATEMIAhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00402
Carbohydrate-deficient glycoprotein syndrome type 1Ahttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00343
Carbohydrate-deficient glycoprotein syndrome type 1Bhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00344
Carbohydrate-Deficient Glycoprotein Syndrome Type Iahttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00343
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE Ia, FORMERLYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00343

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