Defective DPM1 causes DPM1-CDG

Pathway network for the Defective DPM1 causes DPM1-CDG SuperPath

Sources:
  • Reactome
  • PubChem

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Defective DPM1 causes DPM1-CDG SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Developmental and epileptic encephalopathy 36Direct
2Walker-warburg syndromeEnrichmentB3GALNT2, POMGNT2, POMK, POMT1, POMT210.96
3Congenital muscular dystrophy with cerebellar involvementEnrichmentPOMGNT1, POMT1, POMT28.77
4Muscle eye brain diseaseEnrichmentPOMGNT1, POMT1, POMT28.00
5Autosomal recessive limb-girdle muscular dystrophyEnrichmentPOMGNT1, POMT1, POMT27.09
6Muscular dystrophy-dystroglycanopathy , type c, 12EnrichmentPOMK, POMT16.52
7Congenital muscular dystrophy-dystroglycanopathy type aEnrichmentPOMGNT1, POMT26.16
8Muscular dystrophy-dystroglycanopathy , type a, 1EnrichmentPOMT1, POMT25.64
9Congenital muscular dystrophy with intellectual disabilityEnrichmentPOMT1, POMT25.64
10Muscular dystrophy-dystroglycanopathy , type c, 15EnrichmentDPM33.66
11Congenital disorder of glycosylation, type iuEnrichmentDPM23.66
12Muscular dystrophy-dystroglycanopathy , type b, 15EnrichmentDPM33.66
13Muscular dystrophy-dystroglycanopathy , type b, 1EnrichmentPOMT13.29
14Muscular dystrophy-dystroglycanopathy , type c, 1EnrichmentPOMT13.29
15Muscular dystrophy-dystroglycanopathy , type a, 12EnrichmentPOMK3.23
16Muscular dystrophy-dystroglycanopathy , type c, 8EnrichmentPOMGNT23.23
17Muscular dystrophy-dystroglycanopathy , type a, 3EnrichmentPOMGNT12.99
18Muscular dystrophy-dystroglycanopathy , type b, 3EnrichmentPOMGNT12.99
19Muscular dystrophy-dystroglycanopathy , type c, 2EnrichmentPOMT22.99
20Muscular dystrophy-dystroglycanopathy , type a, 2EnrichmentPOMT22.99
21Muscular dystrophy-dystroglycanopathy , type b, 2EnrichmentPOMT22.99
22Retinitis pigmentosa 76EnrichmentPOMGNT12.99
23Congenital muscular dystrophy-dystroglycanopathy type a3EnrichmentPOMGNT12.99
24Muscular dystrophy-dystroglycanopathy , type a, 11EnrichmentB3GALNT22.93
25Congenital muscular dystrophy-dystroglycanopathy type a11EnrichmentB3GALNT22.93
26Congenital nervous system abnormalityEnrichmentPOMGNT1, POMT12.91
27Nervous system diseaseEnrichmentPOMGNT1, POMT12.91
28Muscular dystrophy-dystroglycanopathy , type c, 3EnrichmentPOMGNT12.81
29Muscular dystrophy-dystroglycanopathy , type a, 8EnrichmentPOMGNT22.75
30Congenital muscular dystrophy without intellectual disabilityEnrichmentPOMT12.69
31Muscular dystrophy-dystroglycanopathyEnrichmentPOMGNT12.44
32Congenital muscular dystrophy due to dystroglycanopathyEnrichmentPOMGNT12.44
33HydrocephalusEnrichmentPOMGNT12.11
34Hydrocephalus, congenital, 1EnrichmentPOMT12.08
35MyopathyEnrichmentDPM32.05
36Muscular dystrophyEnrichmentPOMT21.91
37Autosomal recessive non-syndromic intellectual disabilityEnrichmentB3GALNT21.47
38Retinitis pigmentosaEnrichmentPOMGNT10.98
39Hereditary retinal dystrophyEnrichmentPOMGNT10.85
40Fundus dystrophyEnrichmentPOMGNT10.85

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