ERK pathway in Huntington's disease

No Pathway Network information available for ERK pathway in Huntington's disease

Pathways in the ERK pathway in Huntington's disease SuperPath

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

Disorders associated with ERK pathway in Huntington's disease SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome 3EnrichmentHRAS, RAF14.62
2Pilomyxoid astrocytomaEnrichmentNTRK2, RAF14.62
3Melanocytic nevus syndrome, congenitalEnrichmentHRAS, RAF14.50
4Lung non-small cell carcinomaEnrichmentEGFR, HRAS4.20
5Lip and oral cavity carcinomaEnrichmentEGFR, HRAS4.13
6Noonan syndrome and noonan-related syndromeEnrichmentHRAS, RAF13.93
7Noonan syndrome 1EnrichmentHRAS, RAF13.55
8RasopathyEnrichmentHRAS, RAF13.44
9Bladder cancerEnrichmentEGFR, HRAS3.34
10Noonan syndrome 5EnrichmentRAF12.96
11Hypomagnesemia 4, renalEnrichmentEGF2.96
12Cardiomyopathy, dilated, 1nnEnrichmentRAF12.96
13Spinocerebellar ataxia, autosomal recessive 13EnrichmentGRM12.96
14Noonan syndrome 13EnrichmentMAPK12.96
15Developmental and epileptic encephalopathy 58EnrichmentNTRK22.96
16Leopard syndrome 2EnrichmentRAF12.96
17Obesity, hyperphagia, and developmental delayEnrichmentNTRK22.96
18Lopes-maciel-rodan syndromeEnrichmentHTT2.96
19Spinocerebellar ataxia 44EnrichmentGRM12.96
20TrigonitisEnrichmentRAF12.96
21Juvenile huntington diseaseEnrichmentHTT2.96
22Phakomatosis pigmentokeratoticaEnrichmentHRAS2.96
23Chondromyxoid fibromaEnrichmentGRM12.96
24Egf-related primary hypomagnesemia with intellectual disabilityEnrichmentEGF2.96
25Costello syndromeEnrichmentHRAS2.66
26Histiocytoma, angiomatoid fibrousEnrichmentCREB12.66
27Wooly hair nevusEnrichmentHRAS2.66
28Neonatal nephrocutaneous inflammatory syndromeEnrichmentEGFR2.48
29Large congenital melanocytic nevusEnrichmentHRAS2.48
30SpermatocytomaEnrichmentHRAS2.48
31Neonatal inflammatory skin and bowel diseaseEnrichmentEGFR2.48
32Melanoma of soft tissueEnrichmentCREB12.48
33Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS2.35
34Huntington diseaseEnrichmentHTT2.35
35Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.35
36Noonan syndrome with multiple lentiginesEnrichmentRAF12.35
37Epidermolytic nevusEnrichmentHRAS2.35
38Cowden syndrome 1EnrichmentEGFR2.18
39Wilms tumor, aniridia, genitourinary anomalies, and impaired intellectual development syndromeEnrichmentBDNF2.18
40Lung squamous cell carcinomaEnrichmentEGFR2.18
41Nevus, epidermalEnrichmentHRAS2.11
42Thyroid cancer, nonmedullary, 2EnrichmentHRAS2.11
43Squamous cell carcinoma, head and neckEnrichmentEGFR2.11
44Follicular thyroid carcinomaEnrichmentHRAS2.11
45Arteriovenous malformationEnrichmentHRAS2.00
46Adult hepatocellular carcinomaEnrichmentEGF2.00
47Congenital central hypoventilation syndromeEnrichmentBDNF2.00
48Myopathy, x-linked, with excessive autophagyEnrichmentHRAS1.96
49Specific learning disabilityEnrichmentMAPK11.92
50Lung cancer susceptibility 3EnrichmentEGFR1.81
51RhabdomyosarcomaEnrichmentHRAS1.76
52GliosarcomaEnrichmentEGFR1.76
53Giant cell glioblastomaEnrichmentEGFR1.73
54Heart, malformation ofEnrichmentMAPK11.70
55Arteriovenous malformations of the brainEnrichmentEGFR1.68
56Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF11.58
57Hydrops fetalis, nonimmuneEnrichmentHRAS1.55
58Differentiated thyroid carcinomaEnrichmentHRAS1.50
59Non-immune hydrops fetalisEnrichmentHRAS1.47
60Lung cancerEnrichmentEGFR1.46
61Familial hypertrophic cardiomyopathyEnrichmentRAF11.44
62Left ventricular noncompactionEnrichmentRAF11.42
63West syndromeEnrichmentNTRK21.32
64Body mass index quantitative trait locus 11EnrichmentBDNF1.27
65Familial isolated dilated cardiomyopathyEnrichmentRAF11.24
66Undetermined early-onset epileptic encephalopathyEnrichmentNTRK21.22
67Dilated cardiomyopathyEnrichmentRAF11.07
68Ovarian cancerEnrichmentEGFR0.97
69MicrocephalyEnrichmentMAPK10.89
70Complex neurodevelopmental disorderEnrichmentHTT0.89
71Inherited cancer-predisposing syndromeEnrichmentEGFR0.86

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