PI3K/AKT/mTOR - vitamin D3 signaling

No Pathway Network information available for PI3K/AKT/mTOR - vitamin D3 signaling

Pathways in the PI3K/AKT/mTOR - vitamin D3 signaling SuperPath

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

Disorders associated with PI3K/AKT/mTOR - vitamin D3 signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Focal cortical dysplasia, type iiEnrichmentMTOR, TSC1, TSC27.83
2Isolated focal cortical dysplasia type iiEnrichmentMTOR, TSC1, TSC27.83
3Adult hepatocellular carcinomaEnrichmentPIK3CA, TSC1, TSC26.51
4LymphangioleiomyomatosisEnrichmentTSC1, TSC25.60
5Tuberous sclerosis 1EnrichmentTSC1, TSC25.12
6HamartomaEnrichmentTSC1, TSC25.12
7Tuberous sclerosisEnrichmentTSC1, TSC24.82
8HemimegalencephalyEnrichmentMTOR, PIK3CA4.60
9Breast adenocarcinomaEnrichmentAKT1, PIK3CA4.43
10Cowden syndromeEnrichmentAKT1, PIK3CA4.05
11MeningiomaEnrichmentAKT1, PIK3CA3.78
12Behcet syndromeEnrichmentIL10, IL12A3.37
13Ovarian cancerEnrichmentAKT1, PIK3CA, TSC23.25
14Hepatocellular carcinomaEnrichmentPIK3CA, VDR3.25
15Bladder cancerEnrichmentPIK3CA, TSC13.00
16MacrodactylyEnrichmentPIK3CA2.79
17Proteus syndromeEnrichmentAKT12.79
18Megalencephaly, autosomal dominantEnrichmentPIK3CA2.79
19Cowden syndrome 5EnrichmentPIK3CA2.79
20Cerebral cavernous malformations 4EnrichmentPIK3CA2.79
21Graft-versus-host diseaseEnrichmentIL102.79
22Hemifacial myohyperplasiaEnrichmentPIK3CA2.79
23Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.79
24Cowden syndrome 6EnrichmentAKT12.79
25Graham little-piccardi-lassueur syndromeEnrichmentHLA-DRA2.79
26Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.79
27RicketsEnrichmentVDR2.79
28HypospadiasEnrichmentPIK3CA2.79
29Rare venous malformationEnrichmentPIK3CA2.79
30Diaphragmatic eventrationEnrichmentPIK3CA2.79
31Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.79
32Rare combined vascular malformationEnrichmentPIK3CA2.79
33Cavernous lymphangiomaEnrichmentPIK3CA2.79
34Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.79
35Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.79
36Eccrine angiomatous hamartomaEnrichmentPIK3CA2.79
37Macrodactyly of toeEnrichmentPIK3CA2.79
38Hereditary breast carcinomaEnrichmentAKT1, PIK3CA2.64
39Burkitt lymphomaEnrichmentMYC2.49
40Fanconi-bickel syndromeEnrichmentLDHA2.49
41Hypercalcemia, infantile, 1EnrichmentCYP24A12.49
42Keratosis, seborrheicEnrichmentPIK3CA2.49
43Noonan syndrome 8EnrichmentPIK3CA2.49
44Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.49
45Cebalid syndromeEnrichmentMTOR2.49
46Rela fusion-positive ependymomaEnrichmentRELA2.49
47Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.49
48Smith-kingsmore syndromeEnrichmentMTOR2.49
49Autosomal recessive infantile hypercalcemiaEnrichmentCYP24A12.49
50Pompe disease, infantile-onsetEnrichmentPIK3CA2.31
51Polycystic kidney disease, infantile severe, with tuberous sclerosisEnrichmentTSC22.31
52Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA2.31
53Tuberous sclerosis 2EnrichmentTSC22.31
54High-grade b-cell lymphoma double-hit/triple-hitEnrichmentMYC2.31
55Xanthinuria, type iiEnrichmentTSC22.31
56KeratoacanthomaEnrichmentPIK3CA2.31
57Huntington diseaseEnrichmentSLC2A32.19
58Pyruvate dehydrogenase e1-alpha deficiencyEnrichmentPDHA12.19
59Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA2.19
60Cerebrovascular diseaseEnrichmentPIK3CA2.19
61Familial cerebral cavernous malformationsEnrichmentPIK3CA2.19
62Breast cancerEnrichmentAKT1, PIK3CA2.19
63Capillary malformations, congenitalEnrichmentPIK3CA2.09
64Vitamin d-dependent rickets, type 2aEnrichmentVDR2.09
65Colorectal cancerEnrichmentAKT1, PIK3CA2.06
66Klippel-trenaunay-weber syndromeEnrichmentPIK3CA2.01
67Cowden syndrome 1EnrichmentPIK3CA2.01
68Hemihyperplasia, isolatedEnrichmentPIK3CA2.01
69KeratoconusEnrichmentTSC12.01
70Il10-related early-onset inflammatory bowel diseaseEnrichmentIL102.01
71Lung squamous cell carcinomaEnrichmentPIK3CA2.01
72Nevus, epidermalEnrichmentPIK3CA1.95
73Polycystic kidney disease 1 with or without polycystic liver diseaseEnrichmentTSC21.95
74Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.95
75Renal cell carcinoma, papillary, 1EnrichmentMTOR1.95
76Polycystic kidney disease 1EnrichmentTSC21.95
77Gallbladder cancerEnrichmentPIK3CA1.95
78Overgrowth syndromeEnrichmentMTOR1.95
79Rheumatoid arthritisEnrichmentIL101.84
80Arteriovenous malformationEnrichmentPIK3CA1.84
81Primary biliary cholangitisEnrichmentIL12A1.84
82Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.79
83Lung non-small cell carcinomaEnrichmentPIK3CA1.75
84Inherited cancer-predisposing syndromeEnrichmentTSC1, TSC21.72
85Lip and oral cavity carcinomaEnrichmentPIK3CA1.71
86Pulmonary disease, chronic obstructiveEnrichmentVDR1.68
87Renal cell carcinoma, nonpapillaryEnrichmentMTOR1.62
88Lynch syndromeEnrichmentPIK3CA1.62
89Autosomal dominant polycystic kidney diseaseEnrichmentTSC21.62
90Kidney diseaseEnrichmentTSC11.62
91Rare genetic intellectual disabilityEnrichmentMTOR1.62
92Sudden infant death syndromeEnrichmentPDHA11.56
93Human immunodeficiency virus type 1EnrichmentIL101.54
94Endometrial cancerEnrichmentPIK3CA1.47
95Precursor t-cell acute lymphoblastic leukemiaEnrichmentMYC1.44
96Prostate cancerEnrichmentPIK3CA1.34
97Lung cancerEnrichmentPIK3CA1.30
98Systemic lupus erythematosusEnrichmentIL101.21
99Gastric cancerEnrichmentPIK3CA1.17
100West syndromeEnrichmentTSC21.16
101HypertelorismEnrichmentPIK3CA1.09
102Myeloma, multipleEnrichmentRXRA1.06
103Congenital nervous system abnormalityEnrichmentTSC20.80
104Nervous system diseaseEnrichmentTSC20.80
105Autism spectrum disorderEnrichmentTSC20.79

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