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Entry Name Description Category Pathway Gene
H00118 Congenital disorders of glycosylation type I Congenital disorders of glycosylation (CDG) are a group of disorders caused by defects in various genes for N-glycan biosynthesis. CDG type I is defined by mutations in genes encoding enzymes which involves ... Inherited metabolic disorder (CDG1A) PMM2 [HSA:5373] [KO:K17497]
(CDG1B) MPI [HSA:4351] [KO:K01809]
(CDG1C) ALG6 [HSA:29929] [KO:K03848]
(CDG1D) ALG3 [HSA:10195] [KO:K03845]
(CDG1E) DPM1 [HSA:8813] [KO:K00721]
(CDG1F) MPDU1 [HSA:9526] [KO:K09660]
(CDG1G) ALG12 [HSA:79087] [KO:K03847]
(CDG1H) ALG8 [HSA:79053] [KO:K03849]
(CDG1I) ALG2 [HSA:85365] [KO:K03843]
(CDG1J) DPAGT1 [HSA:1798] [KO:K01001]
(CDG1K) ALG1 [HSA:56052] [KO:K03842]
(CDG1L) ALG9 [HSA:79796] [KO:K03846]
(CDG1M) DOLK [HSA:22845] [KO:K00902]
(CDG1N) RFT1 [HSA:91869] [KO:K06316]
(CDG1O) DPM3 [HSA:54344] [KO:K09659]
(CDG1P) ALG11 [HSA:440138] [KO:K03844]
(CDG1Q) SRD5A3 [HSA:79644] [KO:K12345]
(CDG1R) DDOST [HSA:1650] [KO:K12670]
(CDG1S) ALG13 [HSA:79868] [KO:K07432]
(CDG1T) PGM1 [HSA:5236] [KO:K01835]
(CDG1U) DPM2 [HSA:8818] [KO:K09658]
(CDG1WAR) STT3A [HSA:3703] [KO:K07151]
(CDG1X) STT3B [HSA:201595] [KO:K07151]
(CDG1Y) SSR4 [HSA:6748] [KO:K04571]
(CDG1AA) NUS1 [HSA:116150] [KO:K19177]
(CDG1BB) DHDDS [HSA:79947] [KO:K11778]
(CDG1CC) MAGT1 [HSA:84061] [KO:K19478]
(CDG1DD) DHRSX [HSA:207063] [KO:K11170]
(CDG1EE) MAN2B2 [HSA:23324] [KO:K12312]
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