Cell adhesion_Cell-matrix glycoconjugates

No Pathway Network information available for Cell adhesion_Cell-matrix glycoconjugates

Pathways in the Cell adhesion_Cell-matrix glycoconjugates SuperPath

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

Disorders associated with Cell adhesion_Cell-matrix glycoconjugates SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Short stature and advanced bone age with or without early-onset osteoarthritis and/or osteochondritis dissecansEnrichmentACAN2.54
2Tubulointerstitial kidney disease, autosomal dominant 2EnrichmentMUC12.54
3Lipoid proteinosis of urbach and wietheEnrichmentECM12.54
4Lissencephaly 5EnrichmentLAMB12.54
5Deafness, autosomal dominant 56EnrichmentTNC2.54
6Angioedema, hereditary, 4EnrichmentPLG2.54
7Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonusEnrichmentTNR2.54
8Synpolydactyly 2EnrichmentFBLN12.54
9Spondyloepimetaphyseal dysplasia, aggrecan typeEnrichmentACAN2.54
10Spondyloepiphyseal dysplasia, kimberley typeEnrichmentACAN2.54
11Coronary heart disease 6EnrichmentMMP32.54
12Osteochondritis dissecansEnrichmentACAN2.54
13Fbln1-related developmental delay-central nervous system anomaly-syndactyly syndromeEnrichmentFBLN12.54
14Short stature-advanced bone age-early-onset osteoarthritis syndromeEnrichmentACAN2.54
15Cutis laxa, autosomal dominant 1EnrichmentELN2.24
16Cyclic neutropeniaEnrichmentELANE2.24
17Wagner vitreoretinopathyEnrichmentVCAN2.24
18Plasminogen deficiency, type iEnrichmentPLG2.24
19Neutropenia, severe congenital, x-linkedEnrichmentELANE2.24
20Lissencephaly 1EnrichmentLAMB12.24
21Supravalvular aortic stenosisEnrichmentELN2.24
22Epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndromeEnrichmentITGA32.24
23Recessive dystrophic epidermolysis bullosaEnrichmentMMP12.24
24Metaphyseal anadysplasia 2EnrichmentMMP92.24
25Hereditary angioedemaEnrichmentPLG2.24
26Metaphyseal anadysplasiaEnrichmentMMP92.24
27Wagner diseaseEnrichmentVCAN2.24
28Angioedema, hereditary, 1EnrichmentPLG2.07
29Neutropenia, severe congenital, 1, autosomal dominantEnrichmentELANE2.07
30Poretti-boltshauser syndromeEnrichmentLAMA12.07
31Autosomal dominant cutis laxaEnrichmentELN2.07
32Autosomal dominant severe congenital neutropeniaEnrichmentELANE1.84
33Spondyloepiphyseal dysplasia with congenital joint dislocationsEnrichmentACAN1.77
34NeutropeniaEnrichmentELANE1.70
35Stickler syndromeEnrichmentVCAN1.55
36Neural tube defectsEnrichmentITGB11.43
37Multiple sclerosisEnrichmentLAMB11.40
38Human immunodeficiency virus type 1EnrichmentCCL51.30
39Williams-beuren syndromeEnrichmentELN1.25
40Autoinflammatory diseaseEnrichmentELANE1.18
41Cystic fibrosisEnrichmentPLG1.05
42Nephrotic syndromeEnrichmentITGA30.93
43Familial thoracic aortic aneurysm and aortic dissectionEnrichmentELN0.92
44HypertelorismEnrichmentELN0.86
45Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentTNC0.86
46Hereditary retinal dystrophyEnrichmentLAMA1, VCAN0.69
47Fundus dystrophyEnrichmentLAMA1, VCAN0.69

Loading...
Loading...
Loading...