Nitric oxide stimulates guanylate cyclase

No Pathway Network information available for Nitric oxide stimulates guanylate cyclase

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

Disorders associated with Nitric oxide stimulates guanylate cyclase SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Dyskinesia, limb and orofacial, infantile-onsetEnrichmentPDE10A2.93
2Aortic aneurysm, familial thoracic 8EnrichmentPRKG12.93
3Spondylometaphyseal dysplasia, pagnamenta typeEnrichmentPRKG22.93
4Intellectual developmental disorder with paroxysmal dyskinesia or seizuresEnrichmentPDE2A2.93
5Striatal degeneration, autosomal dominant 2EnrichmentPDE10A2.93
6Epilepsy, idiopathic generalized 16EnrichmentKCNMA12.93
7Cerebellar atrophy, developmental delay, and seizuresEnrichmentKCNMA12.93
8Childhood-onset benign chorea with striatal involvementEnrichmentPDE10A2.93
9Pyloric stenosis, infantile hypertrophic, 1EnrichmentNOS12.79
10Moyamoya disease 6 with or without achalasiaEnrichmentGUCY1A12.79
11Moyamoya disease with early-onset achalasiaEnrichmentGUCY1A12.79
12Spinocerebellar ataxia 29EnrichmentITPR12.63
13Hypertension, diastolicEnrichmentKCNMB12.63
14Pigmented nodular adrenocortical disease, primary, 2EnrichmentPDE11A2.63
15Acromesomelic dysplasia 4EnrichmentPRKG22.63
16Liang-wang syndromeEnrichmentKCNMA12.63
17Isolated primary pigmented nodular adrenocortical diseaseEnrichmentPDE11A2.63
18Isolated micronodular adrenocortical diseaseEnrichmentPDE11A2.63
19Gillespie syndromeEnrichmentITPR12.45
20Paroxysmal nonkinesigenic dyskinesia 3 with or without generalized epilepsyEnrichmentKCNMA12.45
21Carney complex variantEnrichmentPDE11A2.33
22Spinocerebellar ataxia 15EnrichmentITPR12.33
23Convulsions, familial infantile, with paroxysmal choreoathetosisEnrichmentPDE2A2.23
24Idiopathic achalasiaEnrichmentNOS12.19
25Spinocerebellar ataxia, autosomal recessive 16EnrichmentITPR12.15
26Alzheimer disease 2EnrichmentNOS32.09
27Pre-eclampsiaEnrichmentNOS32.09
28Paroxysmal dystoniaEnrichmentPDE2A2.08
29Choreatic diseaseEnrichmentPDE2A2.03
30Moyamoya disease 1EnrichmentGUCY1A12.01
31Stroke, ischemicEnrichmentNOS31.79
32Multiple sclerosisEnrichmentITPR11.79
33Anterior segment dysgenesisEnrichmentITPR11.76
34Alzheimer disease, familial, 1EnrichmentNOS31.56
35Hypertension, essentialEnrichmentNOS31.56
36Myocardial infarctionEnrichmentGUCY1A11.45
37MalariaEnrichmentNOS21.44
38Familial thoracic aortic aneurysm and aortic dissectionEnrichmentPRKG11.30
39Spastic ataxiaEnrichmentITPR11.22
40SchizophreniaEnrichmentPDE11A1.17
41Primary ovarian insufficiencyEnrichmentNOS31.04
42Autism spectrum disorderEnrichmentKCNMA10.92

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