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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
181-210 / 356 show all
CUTIS LAXA WITH BONE DYSTROPHYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00371
CUTIS LAXA WITH CONGENITAL DISORDER OF GLYCOSYLATIONhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00371
CUTIS LAXA WITH GROWTH AND DEVELOPMENTAL DELAYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00371
CUTIS LAXA WITH JOINT LAXITY AND RETARDED DEVELOPMENThttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00371
DERMATAN SULFATE PROTEOGLYCANhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00388
Dilated cardiomyopathy with mild or no proximal muscle weaknesshttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00380
Distal myopathy, Nonaka typehttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00386
Distal myopathy with rimmed vacuoleshttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00386
DK1 DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00355
DMDhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00384
DMRVhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00386
DOLICHOL KINASE DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00355
DUCHENNE MUSCULAR DYSTROPHYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00384
DUNDAR SYNDROMEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00634
Dyserythropoietic Anemia, Congenital Type 2http://acgg.asia/db/diseases/gdgdb?con_ui=CON00373
DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IIhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00373
DYSERYTHROPOIETIC ANEMIA, HEMPAS TYPEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00373
EDM4http://acgg.asia/db/diseases/gdgdb?con_ui=CON00398
EDS6http://acgg.asia/db/diseases/gdgdb?con_ui=CON00407
EDS6A, FORMERLYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00407
EDS6B, FORMERLYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00634
EDSMChttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00634
EDSP1http://acgg.asia/db/diseases/gdgdb?con_ui=CON00388
EDS VIhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00407
EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00407
EHLERS-DANLOS SYNDROME, OCULAR-SCOLIOTIC TYPEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00407
Ehlers-Danlos syndrome, type 6http://acgg.asia/db/diseases/gdgdb?con_ui=CON00407
EHLERS-DANLOS SYNDROME, TYPE VIA, FORMERLYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00407
EHLERS-DANLOS SYNDROME, TYPE VIB, FORMERLYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00634
FCMDhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00378

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