Regulation of CDC42 activity

No Pathway Network information available for Regulation of CDC42 activity

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

Disorders associated with Regulation of CDC42 activity SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Developmental and epileptic encephalopathy 8EnrichmentARHGEF92.64
2Autoinflammatory disease, multisystem, with immune dysregulation, x-linkedEnrichmentDOCK112.64
3Nephrotic syndrome, type 8EnrichmentARHGDIA2.64
4Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.64
5Intellectual developmental disorder, x-linked 46EnrichmentARHGEF62.64
6Takenouchi-kosaki syndromeEnrichmentCDC422.64
7Congenital dyserythropoietic anemia type iiibEnrichmentRACGAP12.64
8Familial adenomatous polyposisEnrichmentAPC2.64
9Nocarh syndromeEnrichmentCDC422.64
10Anemia, congenital dyserythropoietic, type iiib, autosomal recessiveEnrichmentRACGAP12.64
11Gardner syndromeEnrichmentAPC2.64
125q22 microdeletion syndromeEnrichmentAPC2.64
13Attenuated familial adenomatous polyposisEnrichmentAPC2.64
14Anemia, congenital dyserythropoietic, type iiiaEnrichmentRACGAP12.34
15Adams-oliver syndrome 2EnrichmentDOCK62.34
16Periampullary adenomaEnrichmentAPC2.34
17Gastric adenocarcinoma and proximal polyposis of the stomachEnrichmentAPC2.34
18Immune system diseaseEnrichmentCDC422.34
19Paget's disease of boneEnrichmentDOCK62.34
20Aarskog syndromeEnrichmentFGD12.34
21Cataract 48EnrichmentDNMBP2.34
22Desmoid disease, hereditaryEnrichmentAPC2.16
23Aarskog-scott syndromeEnrichmentFGD12.16
24Intellectual developmental disorder, x-linked, syndromic, claes-jensen typeEnrichmentFGD12.16
25Hypercholanemia, familial 1EnrichmentDOCK62.16
26Adams-oliver syndrome 1EnrichmentDOCK62.16
27Cenani-lenz syndactyly syndromeEnrichmentAPC2.16
28Desmoid tumorEnrichmentAPC2.16
29Colon adenocarcinomaEnrichmentAPC2.16
30Syndromic x-linked intellectual disability claes-jensen typeEnrichmentFGD12.16
31Apc-associated polyposis conditionsEnrichmentAPC2.16
32Intellectual developmental disorder, autosomal dominant 1EnrichmentITSN12.04
33CraniopharyngiomaEnrichmentAPC2.04
34Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCDC422.04
35Familial adenomatous polyposis 1EnrichmentAPC1.94
36Adams-oliver syndromeEnrichmentDOCK61.80
37Moyamoya angiopathyEnrichmentARHGEF251.80
38Colonic benign neoplasmEnrichmentAPC1.69
39Hypercholesterolemia, familial, 1EnrichmentDOCK61.53
40MedulloblastomaEnrichmentAPC1.50
41Familial hypercholesterolemiaEnrichmentDOCK61.47
42Cataract 44EnrichmentDNMBP1.42
43Esophageal atresia/tracheoesophageal fistulaEnrichmentITSN11.37
44HepatoblastomaEnrichmentAPC1.33
45Hepatocellular carcinomaEnrichmentAPC1.31
46Genetic steroid-resistant nephrotic syndromeEnrichmentARHGDIA1.13
47Non-syndromic x-linked intellectual disabilityEnrichmentARHGEF61.10
48Gastric cancerEnrichmentAPC1.03
49Hereditary breast carcinomaEnrichmentAPC1.02
50Autosomal dominant non-syndromic intellectual disabilityEnrichmentITSN10.97
51Breast cancerEnrichmentAPC0.80
52Colorectal cancerEnrichmentAPC0.74
53Ovarian cancerEnrichmentAPC0.68
54Inherited cancer-predisposing syndromeEnrichmentAPC0.58

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