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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
301-330 / 356 show all
NIEMANN-PICK DISEASE, TYPE Chttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00089
NIEMANN-PICK DISEASE WITH CHOLESTEROL ESTERIFICATION BLOCKhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00089
NIEMANN-PICK DISEASE WITHOUT SPHINGOMYELINASE DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00089
Niemann-Pick病C1型@jahttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00089
NMhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00386
NONAKA DISTAL MYOPATHYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00386
NPChttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00089
NPC1http://acgg.asia/db/diseases/gdgdb?con_ui=CON00089
Ocular colobomas, ichthyosis, brain malformations and endocrine abnormalitieshttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00622
OSTEOGENESIS IMPERFECTA WITH CONGENITAL JOINT CONTRACTUREShttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00408
PAROXYSMAL NOCTURNAL HEMOGLOBINURIAhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00414
PDS, DEFECTIVE BIOSYNTHESIS OFhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00388
PHOSPHOMANNOMUTASE 2 DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00343
PHPTChttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00402
PNHhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00414
PNH1http://acgg.asia/db/diseases/gdgdb?con_ui=CON00414
PPCA DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00023
PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00632
Progeroid variant of Ehlers-Danlos syndromehttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00388
PROTECTIVE PROTEIN/CATHEPSIN A DEFICIENCYhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00023
PROTEIN-LOSING ENTEROPATHY-HEPATIC FIBROSIS SYNDROMEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00344
PROTEODERMATAN SULFATE, DEFECTIVE BIOSYNTHESIS OFhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00388
QSMhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00385
Rambam Hasharon syndromehttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00360
RAMBAM-HASHARON SYNDROMEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00360
RHShttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00360
SAGUENAY-LAC SAINT-JEAN SYNDROMEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00344
SLSJ SYNDROMEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00344
SULFATIDOSIS, JUVENILE, AUSTIN TYPEhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00078
TEUTSCHLAENDER DISEASE, FAMILIALhttp://acgg.asia/db/diseases/gdgdb?con_ui=CON00402

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