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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
241-270 / 356 show all
JAEKEN SYNDROMEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00343
LAD2http://acgg.asia/db/diseases/gdgdb?con_ui=CON00360
Leukocyte adhesion deficiency, type 2http://acgg.asia/db/diseases/gdgdb?con_ui=CON00360
LEUKOCYTE ADHESION DEFICIENCY, TYPE IIhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00360
LGMD2Ihttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00382
LGMD2Mhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00379
Limb-girdle muscular dystrophy type 2Ihttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00382
Limb-girdle muscular dystrophy type 2Mhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00379
LIPOCALCINOGRANULOMATOSIShttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00402
LYSOSOMAL ALPHA-D-MANNOSIDASE DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00008
LYSOSOMAL BETA-MANNOSIDASE DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00011
LYSOSOMAL PROTECTIVE PROTEIN DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00023
MABRY SYNDROMEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00635
MACULAR CORNEAL DYSTROPHY, TYPE Ihttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00391
MANNOSEPHOSPHATE ISOMERASE DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00344
MANSAhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00008
MANSBhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00011
MCDhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00391
MCDC1http://acgg.asia/db/diseases/gdgdb?con_ui=CON00391
MDC1Chttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00381
MDC1Dhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00383
MDDGA1 and MDDGA2http://acgg.asia/db/diseases/gdgdb?con_ui=CON00376
MDDGA3http://acgg.asia/db/diseases/gdgdb?con_ui=CON00377
MDDGA4http://acgg.asia/db/diseases/gdgdb?con_ui=CON00378
MDDGB5http://acgg.asia/db/diseases/gdgdb?con_ui=CON00381
MDDGB6http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383
MDDGC4http://acgg.asia/db/diseases/gdgdb?con_ui=CON00379
MDDGC5http://acgg.asia/db/diseases/gdgdb?con_ui=CON00382
MEB 病@jahttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00377
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 22http://acgg.asia/db/diseases/gdgdb?con_ui=CON00369

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