miRs in Muscle Cell Differentiation

No Pathway Network information available for miRs in Muscle Cell Differentiation

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

Disorders associated with miRs in Muscle Cell Differentiation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Ellis-van creveld syndromeEnrichmentPRKACA, PRKACB3.66
2Acrodysostosis 1 with or without hormone resistanceEnrichmentPRKAR1A2.60
3Carney complex, type 1EnrichmentPRKAR1A2.60
4Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.60
5Cardioacrofacial dysplasia 2EnrichmentPRKACB2.60
6Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C2.60
7Myxoma, intracardiacEnrichmentPRKAR1A2.60
8Coronary artery disease, autosomal dominant, 1EnrichmentMEF2A2.60
9Spinocerebellar ataxia 14EnrichmentPRKCG2.60
10Ophthalmoplegia, external, with rib and vertebral anomaliesEnrichmentMYF52.60
11Congenital myopathy 19EnrichmentPAX72.60
12Congenital myopathy 17EnrichmentMYOD12.60
13Pigmented nodular adrenocortical disease, primary, 4EnrichmentPRKACA2.60
14Congenital heart defects and ectodermal dysplasiaEnrichmentPRKD12.60
15Cardioacrofacial dysplasia 1EnrichmentPRKACA2.60
16Prkar1b-related neurodegenerative dementia with intermediate filamentsEnrichmentPRKAR1B2.60
175q14.3 microdeletion syndromeEnrichmentMEF2C2.60
18Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C2.60
19Mef2c-related disorderEnrichmentMEF2C2.60
20Malignant epithelial tumor of salivary glandsEnrichmentPRKD12.60
21Amelogenesis imperfecta, type igEnrichmentPRKAR1A2.30
22Pigmented nodular adrenocortical disease, primary, 1EnrichmentPRKAR1A2.30
23Bleeding disorder, platelet-type, 19EnrichmentPRKACG2.30
24Marbach-schaaf neurodevelopmental syndromeEnrichmentPRKAR1B2.30
25Usher syndrome, type ivEnrichmentPRKAR1A2.30
26AcrodysostosisEnrichmentPRKAR1A2.30
27Fibrolamellar carcinomaEnrichmentPRKACA2.30
28Ciliary dyskinesia, primary, 18EnrichmentPRKAR1B2.30
29Isolated primary pigmented nodular adrenocortical diseaseEnrichmentPRKAR1A2.30
30Weaver syndromeEnrichmentEZH22.12
31Carney complex variantEnrichmentPRKAR1A2.00
32Arrhythmogenic right ventricular dysplasia, familial, 10EnrichmentPRKAR1A2.00
33Hereditary ataxiaEnrichmentPRKCG2.00
34Rhabdomyosarcoma 2EnrichmentPAX71.90
35Myopathy, centronuclear, 1EnrichmentMYOD11.83
36Adrenocortical carcinomaEnrichmentPRKAR1A1.83
37Inflammatory bowel disease 1EnrichmentPRKCQ1.65
38Stroke, ischemicEnrichmentPRKCH1.61
39Acute promyelocytic leukemiaEnrichmentPRKAR1A1.49
40Chromosome 1p36 deletion syndromeEnrichmentPRKCZ1.49
41Inherited cancer-predisposing syndromeEnrichmentEZH2, PRKAR1A1.37
42ScoliosisEnrichmentMYF51.23
43Fetal akinesia deformation sequence 1EnrichmentMYOD11.05
44Distal arthrogryposisEnrichmentMYOD11.00
45Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C0.87
46Primary ciliary dyskinesiaEnrichmentPRKAR1B0.76
47Autism spectrum disorderEnrichmentMEF2C0.62

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