Effects of PIP2 hydrolysis

No Pathway Network information available for Effects of PIP2 hydrolysis

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

Disorders associated with Effects of PIP2 hydrolysis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Neuroocular syndrome 2, paroxysmal typeEnrichmentDAGLA3.43
2Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataractEnrichmentABHD123.13
3Anhidrosis, isolated, with normal sweat glandsEnrichmentITPR22.72
4Focal segmental glomerulosclerosis 2EnrichmentTRPC62.72
5Bleeding disorder, platelet-type, 18EnrichmentRASGRP22.72
6Spinocerebellar ataxia 41EnrichmentTRPC32.72
7Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.72
8Immunodeficiency 64 with lymphoproliferationEnrichmentRASGRP12.72
9Charcot-marie-tooth disease, demyelinating, type 1jEnrichmentITPR32.72
10Immunodeficiency 133 with ectodermal dysplasia with or without peripheral neuropathyEnrichmentITPR32.72
11Immunodeficiency 64EnrichmentRASGRP12.72
12Ebv-induced lymphoproliferative disease due to rasgrp1 deficiencyEnrichmentRASGRP12.72
13Nephrotic syndromeEnrichmentDGKE, TRPC62.52
14Autosomal dominant cerebellar ataxiaEnrichmentDAGLA2.48
15Spinocerebellar ataxia 29EnrichmentITPR12.42
16Nephrotic syndrome, type 7EnrichmentDGKE2.42
17Hemolytic-uremic syndromeEnrichmentDGKE2.42
18Gillespie syndromeEnrichmentITPR12.24
19Spinocerebellar ataxia 15EnrichmentITPR12.12
20Cone dystrophyEnrichmentABHD122.05
21Hemolytic uremic syndrome, atypical 1EnrichmentDGKE2.02
22Spinocerebellar ataxia, autosomal recessive 16EnrichmentITPR11.94
23Stroke, ischemicEnrichmentPRKCH1.72
24Congenital long qt syndromeEnrichmentITPR31.64
25Multiple sclerosisEnrichmentITPR11.58
26Anterior segment dysgenesisEnrichmentITPR11.55
27Atypical hemolytic-uremic syndromeEnrichmentDGKE1.55
28Focal segmental glomerulosclerosisEnrichmentTRPC61.42
29Severe covid-19EnrichmentDGKE1.27
30Long qt syndrome 1EnrichmentITPR31.25
31Genetic steroid-resistant nephrotic syndromeEnrichmentTRPC61.20
32Spastic ataxiaEnrichmentITPR11.01
33Hereditary retinal dystrophyEnrichmentABHD120.99
34Fundus dystrophyEnrichmentABHD120.99

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