Cannabinoid receptor signaling

No Pathway Network information available for Cannabinoid receptor signaling

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

Disorders associated with Cannabinoid receptor signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Polysubstance abuseEnrichmentFAAH4.13
2Ellis-van creveld syndromeEnrichmentPRKACA, PRKACB4.13
3Acrodysostosis 1 with or without hormone resistanceEnrichmentPRKAR1A2.83
4Drug metabolism, poor, cyp2c19-relatedEnrichmentCYP2C192.83
5Carney complex, type 1EnrichmentPRKAR1A2.83
6Deafness, autosomal recessive 44EnrichmentADCY12.83
7Neuroocular syndrome 2, paroxysmal typeEnrichmentDAGLA2.83
8Retinitis pigmentosa 85EnrichmentAHR2.83
9Foveal hypoplasia 3EnrichmentAHR2.83
10Cardioacrofacial dysplasia 2EnrichmentPRKACB2.83
11Myxoma, intracardiacEnrichmentPRKAR1A2.83
12Pigmented nodular adrenocortical disease, primary, 4EnrichmentPRKACA2.83
13Cardioacrofacial dysplasia 1EnrichmentPRKACA2.83
14Vitamin d-dependent rickets, type 3EnrichmentCYP3A42.83
15Prkar1b-related neurodegenerative dementia with intermediate filamentsEnrichmentPRKAR1B2.83
16Acute encephalopathy with biphasic seizures and late reduced diffusionEnrichmentADORA2A2.83
17Amelogenesis imperfecta, type igEnrichmentPRKAR1A2.53
18Pigmented nodular adrenocortical disease, primary, 1EnrichmentPRKAR1A2.53
19Bleeding disorder, platelet-type, 19EnrichmentPRKACG2.53
20Marbach-schaaf neurodevelopmental syndromeEnrichmentPRKAR1B2.53
21Usher syndrome, type ivEnrichmentPRKAR1A2.53
22AcrodysostosisEnrichmentPRKAR1A2.53
23Fibrolamellar carcinomaEnrichmentPRKACA2.53
24Ciliary dyskinesia, primary, 18EnrichmentPRKAR1B2.53
25Isolated primary pigmented nodular adrenocortical diseaseEnrichmentPRKAR1A2.53
26Coumarin resistanceEnrichmentCYP2C92.35
27Carney complex variantEnrichmentPRKAR1A2.23
28Arrhythmogenic right ventricular dysplasia, familial, 10EnrichmentPRKAR1A2.23
29Adrenocortical carcinomaEnrichmentPRKAR1A2.05
30Autosomal dominant cerebellar ataxiaEnrichmentDAGLA1.88
31Acute promyelocytic leukemiaEnrichmentPRKAR1A1.72
32Primary ciliary dyskinesiaEnrichmentPRKAR1B0.97
33Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentADCY10.91
34Inherited cancer-predisposing syndromeEnrichmentPRKAR1A0.75
35Retinitis pigmentosaEnrichmentAHR0.57

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