Trk receptor signaling mediated by the MAPK pathway

No Pathway Network information available for Trk receptor signaling mediated by the MAPK pathway

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

Disorders associated with Trk receptor signaling mediated by the MAPK pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome and noonan-related syndromeEnrichmentBRAF, MAP2K1, RAF1, RIT17.78
2Noonan syndrome 1EnrichmentBRAF, MAP2K1, RAF1, RIT16.97
3RasopathyEnrichmentBRAF, MAP2K1, RAF1, RIT16.74
4Langerhans cell histiocytosisEnrichmentBRAF, MAP2K14.94
5Cardiofaciocutaneous syndrome 1EnrichmentBRAF, MAP2K14.64
6Cardiofaciocutaneous syndromeEnrichmentBRAF, MAP2K14.64
7Noonan syndrome with multiple lentiginesEnrichmentBRAF, RAF14.64
8Pilomyxoid astrocytomaEnrichmentBRAF, RAF14.10
9Melanocytic nevus syndrome, congenitalEnrichmentBRAF, RAF13.97
10Lung non-small cell carcinomaEnrichmentBRAF, MAP2K13.68
11Scoliosis, isolated 1EnrichmentMAPK73.53
12Noonan syndrome 5EnrichmentRAF12.70
13Melorheostosis, isolatedEnrichmentMAP2K12.70
14Noonan syndrome 7EnrichmentBRAF2.70
15Leopard syndrome 3EnrichmentBRAF2.70
16Cardiomyopathy, dilated, 1nnEnrichmentRAF12.70
17Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.70
18Lissencephaly 7 with cerebellar hypoplasiaEnrichmentCDK52.70
19Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.70
20Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C2.70
21LymphangiomaEnrichmentBRAF2.70
22Phace associationEnrichmentBRAF2.70
23MelorheostosisEnrichmentMAP2K12.70
24Leopard syndrome 2EnrichmentRAF12.70
25TrigonitisEnrichmentRAF12.70
265q14.3 microdeletion syndromeEnrichmentMEF2C2.70
27Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C2.70
28Syringocystadenoma papilliferumEnrichmentBRAF2.70
29GangliogliomaEnrichmentBRAF2.70
30Nongerminomatous germ cell tumorEnrichmentBRAF2.70
31Phace syndromeEnrichmentBRAF2.70
32Mef2c-related disorderEnrichmentMEF2C2.70
33Classic hairy cell leukemiaEnrichmentBRAF2.70
34Pulmonic stenosisEnrichmentBRAF2.40
35Histiocytoma, angiomatoid fibrousEnrichmentCREB12.40
36Noonan syndrome 8EnrichmentRIT12.40
37Ataxia-telangiectasiaEnrichmentBRAF2.22
38Tethered spinal cord syndromeEnrichmentBRAF2.22
39Melanoma of soft tissueEnrichmentCREB12.22
40Thyroid cancer, nonmedullary, 1EnrichmentBRAF2.10
41Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentRIT12.10
42Congenital generalized lipodystrophyEnrichmentFOS2.10
43CraniopharyngiomaEnrichmentBRAF2.10
44Newborn respiratory distress syndromeEnrichmentBRAF2.10
45Histiocytoid hemangiomaEnrichmentFOS2.00
46Dilated cardiomyopathyEnrichmentBRAF, RAF11.96
47Wilms tumor 5EnrichmentBRAF1.92
48Thyroid cancer, nonmedullary, 2EnrichmentBRAF1.86
49Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K11.86
50Noonan syndrome 3EnrichmentRAF11.86
51Gallbladder cancerEnrichmentBRAF1.86
52Follicular thyroid carcinomaEnrichmentBRAF1.86
53Lymphoma, non-hodgkin, familialEnrichmentBRAF1.80
54Cardiomyopathy, familial hypertrophic, 4EnrichmentBRAF1.75
55Arteriovenous malformationEnrichmentMAP2K11.75
56Primary hyperaldosteronismEnrichmentBRAF1.75
57Ventricular septal defectEnrichmentBRAF1.75
58Autism spectrum disorderEnrichmentMAP2K1, MEF2C1.71
59Myopathy, x-linked, with excessive autophagyEnrichmentMAP2K11.70
60MelanomaEnrichmentBRAF1.70
61Lip and oral cavity carcinomaEnrichmentBRAF1.63
62Lung cancer susceptibility 3EnrichmentBRAF1.56
63Heart diseaseEnrichmentRIT11.56
64Wilms tumor 1EnrichmentBRAF1.53
65Melanoma, cutaneous malignant 1EnrichmentBRAF1.48
66Dandy-walker syndromeEnrichmentBRAF1.48
67Arteriovenous malformations of the brainEnrichmentBRAF1.43
68Diffuse large b-cell lymphomaEnrichmentBRAF1.43
69Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.33
70Hydrops fetalis, nonimmuneEnrichmentRIT11.30
71Differentiated thyroid carcinomaEnrichmentBRAF1.25
72Non-immune hydrops fetalisEnrichmentRIT11.22
73Lung cancerEnrichmentBRAF1.21
74Familial hypertrophic cardiomyopathyEnrichmentRAF11.20
75Left ventricular noncompactionEnrichmentRAF11.17
76HypertelorismEnrichmentRIT11.01
77Familial isolated dilated cardiomyopathyEnrichmentRAF11.00
78Myeloma, multipleEnrichmentBRAF0.98
79Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C0.96
80Colorectal cancerEnrichmentBRAF0.80

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