SRF and miRs in smooth muscle differentiation and proliferation

No Pathway Network information available for SRF and miRs in smooth muscle differentiation and proliferation

Pathways in the SRF and miRs in smooth muscle differentiation and proliferation SuperPath

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

Disorders associated with SRF and miRs in smooth muscle differentiation and proliferation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Atrial septal defect 7 with or without atrioventricular conduction defectsEnrichmentNKX2-53.09
2Hypothyroidism, congenital, nongoitrous, 5EnrichmentNKX2-53.09
3Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3EnrichmentCCND23.09
4Megabladder, congenitalEnrichmentMYOCD3.09
5Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C3.09
6Coronary artery disease, autosomal dominant, 1EnrichmentMEF2A3.09
7Ventricular septal defect 3EnrichmentNKX2-53.09
8Hypoplastic left heart syndrome 2EnrichmentNKX2-53.09
95q14.3 microdeletion syndromeEnrichmentMEF2C3.09
10Aortic arch interruptionEnrichmentNKX2-53.09
11Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C3.09
12Atrial heart septal defect 7EnrichmentNKX2-53.09
13Mef2c-related disorderEnrichmentMEF2C3.09
14Familial isolated congenital aspleniaEnrichmentNKX2-52.79
15Deletion 5q35EnrichmentNKX2-52.79
16Prune belly syndromeEnrichmentMYOCD2.61
17Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentCCND22.49
18Hereditary progressive cardiac conduction defectEnrichmentNKX2-52.49
19Persistent truncus arteriosusEnrichmentNKX2-52.39
20Conotruncal heart malformationsEnrichmentNKX2-52.31
21Double outlet right ventricleEnrichmentNKX2-52.31
22Hypothyroidism, congenital, nongoitrous, 2EnrichmentNKX2-52.25
23Hypoplastic left heart syndromeEnrichmentNKX2-52.19
24Atrial heart septal defectEnrichmentNKX2-52.05
25Interatrial communicationEnrichmentNKX2-52.05
26Aortic valve disease 1EnrichmentNKX2-51.98
27Heart diseaseEnrichmentNKX2-51.95
28Patent foramen ovaleEnrichmentNKX2-51.84
29Familial atrial fibrillationEnrichmentNKX2-51.71
30Tetralogy of fallotEnrichmentNKX2-51.68
31Left ventricular noncompactionEnrichmentNKX2-51.55
32Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C1.34
33Dilated cardiomyopathyEnrichmentNKX2-51.20
34Autism spectrum disorderEnrichmentMEF2C1.07

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