Development_Glucocorticoid receptor signaling

No Pathway Network information available for Development_Glucocorticoid receptor signaling

Pathways in the Development_Glucocorticoid receptor signaling SuperPath

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

Disorders associated with Development_Glucocorticoid receptor signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Aortic aneurysmEnrichmentSMAD3, TGFBR14.27
2Rubinstein-taybi syndrome 1EnrichmentCREBBP, EP3003.88
3Chromosome 16p13.3 deletion syndrome, proximalEnrichmentCREBBP, EP3003.88
4Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.73
5Loeys-dietz syndromeEnrichmentSMAD3, TGFBR13.50
6Rare genetic intellectual disabilityEnrichmentCREBBP, EP3003.04
7Multiple self-healing squamous epitheliomaEnrichmentTGFBR12.52
8Glucocorticoid resistance, generalizedEnrichmentNR3C12.52
9Even-plus syndromeEnrichmentHSPA92.52
10Anemia, sideroblastic, 4EnrichmentHSPA92.52
11Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominantEnrichmentSTAT5B2.52
12Immunodeficiency 92EnrichmentREL2.52
13Orofacial cleft 10EnrichmentSUMO12.52
14Plasminogen activator inhibitor-1 deficiencyEnrichmentSERPINE12.52
15Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.52
16Immunodeficiency 53EnrichmentRELB2.52
17Menke-hennekam syndrome 1EnrichmentCREBBP2.52
18Rubinstein-taybi syndrome due to 16p13.3 microdeletionEnrichmentCREBBP2.52
19Menke-hennekam syndromeEnrichmentCREBBP2.52
20Congenital plasminogen activator inhibitor type 1 deficiencyEnrichmentSERPINE12.52
21Galactosemia iiEnrichmentNR3C12.22
22Metaphyseal dysplasia, spahr typeEnrichmentMMP132.22
23Thumb deformityEnrichmentCREBBP2.22
24Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessiveEnrichmentSTAT5B2.22
25Spondyloepimetaphyseal dysplasia, missouri typeEnrichmentMMP132.22
26Loeys-dietz syndrome 2EnrichmentTGFBR12.22
27Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA2.22
28Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.22
29Immunodeficiency, common variable, 10EnrichmentNFKB22.22
30Loeys-dietz syndrome 3EnrichmentSMAD32.22
31Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.22
32Menke-hennekam syndrome 2EnrichmentEP3002.22
33Rela fusion-positive ependymomaEnrichmentRELA2.22
34Acute myeloid leukemia with kat6a-crebbp fusionEnrichmentCREBBP2.22
35Ectodermal dysplasia and immune deficiencyEnrichmentNFKBIA2.22
36Autosomal recessive sideroblastic anemiaEnrichmentHSPA92.22
37Metaphyseal anadysplasiaEnrichmentMMP132.22
38Common variable immunodeficiency 12EnrichmentNFKB12.22
39Laron syndrome with immunodeficiencyEnrichmentSTAT5B2.22
40Familial thoracic aortic aneurysm and aortic dissectionEnrichmentSMAD3, TGFBR12.11
41Nasopharyngeal carcinomaEnrichmentNFKBIA2.04
42Tethered spinal cord syndromeEnrichmentCREBBP2.04
43Loeys-dietz syndrome 1EnrichmentTGFBR12.04
44Intraocular pressure quantitative trait locusEnrichmentCREBBP2.04
45Immunodeficiency, common variable, 1EnrichmentNFKB21.92
46Congenital generalized lipodystrophyEnrichmentFOS1.92
47Pseudomyogenic hemangioendotheliomaEnrichmentSERPINE11.92
48Rubinstein-taybi syndrome 2EnrichmentEP3001.82
49Histiocytoid hemangiomaEnrichmentFOS1.82
50Congenital anomalies of kidney and urinary tract 1EnrichmentTRAP11.74
51HypertrichosisEnrichmentCREBBP1.74
52Classic ehlers-danlos syndromeEnrichmentTGFBR11.74
53Charge syndromeEnrichmentEP3001.57
54Primary hyperaldosteronismEnrichmentNR3C11.57
55Familial thoracic aortic aneurysm and dissectionEnrichmentSMAD31.57
56Marfan syndromeEnrichmentTGFBR11.53
57Ciliary dyskinesia, primary, 3EnrichmentNFKB11.53
58Pectus excavatumEnrichmentTGFBR11.48
59Acute promyelocytic leukemiaEnrichmentSTAT5B1.41
60Aortic aneurysm, familial thoracic 1EnrichmentSMAD31.38
61Heart diseaseEnrichmentCREBBP1.38
62Polydactyly, postaxial, type a1EnrichmentEP3001.35
63Corpus callosum, agenesis ofEnrichmentCREBBP1.35
64Isolated corpus callosum agenesisEnrichmentCREBBP1.35
65Intellectual disability-hypoplastic corpus callosum-preauricular tag syndromeEnrichmentCREBBP1.35
66GliosarcomaEnrichmentNFKBIA1.33
67Giant cell glioblastomaEnrichmentNFKBIA1.30
68Diffuse large b-cell lymphomaEnrichmentCREBBP1.25
69Ehlers-danlos syndromeEnrichmentSMAD31.25
70Tooth agenesisEnrichmentSUMO11.19
71ScoliosisEnrichmentCREBBP1.15
72Connective tissue diseaseEnrichmentSMAD31.03
73CakutEnrichmentTRAP11.01
74Myeloma, multipleEnrichmentCREBBP0.81
75AutismEnrichmentCREBBP0.71
76Breast cancerEnrichmentJUN0.69
77Colorectal cancerEnrichmentEP3000.63
78Congenital nervous system abnormalityEnrichmentCREBBP0.56
79Nervous system diseaseEnrichmentCREBBP0.56
80MicrocephalyEnrichmentEP3000.51

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