Retinoic acid receptors-mediated signaling

No Pathway Network information available for Retinoic acid receptors-mediated signaling

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

Disorders associated with Retinoic acid receptors-mediated signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1RicketsEnrichmentVDR3.66
2Vitamin d-dependent rickets, type 2aEnrichmentVDR2.96
3Proteus syndromeEnrichmentAKT12.75
4Spinocerebellar ataxia 14EnrichmentPRKCG2.75
5Cowden syndrome 6EnrichmentAKT12.75
6Pigmented nodular adrenocortical disease, primary, 4EnrichmentPRKACA2.75
7Cardioacrofacial dysplasia 1EnrichmentPRKACA2.75
8Congenital anomalies of kidney and urinary tract 3EnrichmentNRIP12.75
9Pulmonary disease, chronic obstructiveEnrichmentVDR2.54
10Acute promyelocytic leukemiaEnrichmentRARA2.54
11Fibrolamellar carcinomaEnrichmentPRKACA2.45
12Myeloma, multipleEnrichmentNCOR2, RXRA2.36
13Hepatocellular carcinomaEnrichmentVDR2.31
14Wieacker-wolff syndromeEnrichmentCCNH2.28
15Hereditary ataxiaEnrichmentPRKCG2.15
16Capillary malformations, congenitalEnrichmentCCNH2.05
17Klippel-trenaunay-weber syndromeEnrichmentCCNH1.98
18Telangiectasia, hereditary hemorrhagic, type 1EnrichmentCCNH1.98
19Hemangioma, capillary infantileEnrichmentCCNH1.98
20Basal cell carcinoma 1EnrichmentCCNH1.98
21Breast adenocarcinomaEnrichmentAKT11.98
22Capillary malformation-arteriovenous malformation 1EnrichmentCCNH1.91
23Hereditary hemorrhagic telangiectasiaEnrichmentCCNH1.91
24Ellis-van creveld syndromeEnrichmentPRKACA1.80
25Arteriovenous malformationEnrichmentCCNH1.80
26Cowden syndromeEnrichmentAKT11.80
27Myopathy, x-linked, with excessive autophagyEnrichmentCCNH1.76
28MeningiomaEnrichmentAKT11.68
29CakutEnrichmentNRIP11.23
30Hereditary breast carcinomaEnrichmentAKT11.12
31Breast cancerEnrichmentAKT10.90
32Colorectal cancerEnrichmentAKT10.84
33Ovarian cancerEnrichmentAKT10.78

Loading...
Loading...
Loading...