Signaling by EGFR

Pathway network for the Signaling by EGFR SuperPath

Sources:
  • Reactome

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

Disorders associated with Signaling by EGFR SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome and noonan-related syndromeEnrichmentCBL, HRAS, KRAS, NRAS, PTPN11, SOS110.44
2Noonan syndrome 1EnrichmentCBL, HRAS, KRAS, NRAS, PTPN11, SOS19.55
3Lung non-small cell carcinomaEnrichmentEGFR, HRAS, KRAS, NRAS, PIK3CA9.45
4RasopathyEnrichmentCBL, HRAS, KRAS, NRAS, PTPN11, SOS19.24
5Nevus, epidermalEnrichmentHRAS, KRAS, NRAS, PIK3CA8.14
6Noonan syndrome 3EnrichmentHRAS, KRAS, PTPN11, SOS18.14
7Juvenile myelomonocytic leukemiaEnrichmentCBL, KRAS, NRAS, PTPN117.00
8Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS, KRAS, NRAS6.65
9Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCBL, CDC42, PTPN116.65
10Lung squamous cell carcinomaEnrichmentEGFR, KRAS, PIK3CA5.95
11Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R15.35
12Bladder cancerEnrichmentEGFR, HRAS, KRAS, PIK3CA5.34
13Lip and oral cavity carcinomaEnrichmentEGFR, HRAS, PIK3CA4.92
14Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS, NRAS4.82
15Colorectal cancerEnrichmentNRAS, PIK3CA, PIK3R1, PTPN12, SRC4.66
16Cowden syndrome 1EnrichmentEGFR, PIK3CA4.66
17Large congenital melanocytic nevusEnrichmentHRAS, NRAS4.35
18Neonatal inflammatory skin and bowel diseaseEnrichmentADAM17, EGFR4.35
19Adult hepatocellular carcinomaEnrichmentEGF, PIK3CA4.28
20Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS, NRAS4.05
21Differentiated thyroid carcinomaEnrichmentHRAS, KRAS, NRAS3.72
22Breast adenocarcinomaEnrichmentKRAS, PIK3CA3.65
23Non-immune hydrops fetalisEnrichmentHRAS, KRAS, PTPN113.63
24Lung cancerEnrichmentEGFR, KRAS, PIK3CA3.59
25Thyroid cancer, nonmedullary, 2EnrichmentHRAS, NRAS3.51
26Capillary malformation-arteriovenous malformation 1EnrichmentKRAS, PIK3CA3.51
27Leukemia, chronic myeloidEnrichmentKRAS, NRAS3.51
28Gallbladder cancerEnrichmentKRAS, PIK3CA3.51
29Follicular thyroid carcinomaEnrichmentHRAS, NRAS3.51
30Melanocytic nevus syndrome, congenitalEnrichmentHRAS, NRAS3.38
31Leukemia, acute myeloidEnrichmentKRAS, NRAS, SH3GL13.30
32Arteriovenous malformationEnrichmentHRAS, PIK3CA3.28
33Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, PIK3CA3.18
34MacrodactylyEnrichmentPIK3CA2.90
35MetachondromatosisEnrichmentPTPN112.90
36Deafness, autosomal recessive 26EnrichmentGAB12.90
37Hypomagnesemia 4, renalEnrichmentEGF2.90
38Megalencephaly, autosomal dominantEnrichmentPIK3CA2.90
39Leopard syndrome 1EnrichmentPTPN112.90
40Cowden syndrome 5EnrichmentPIK3CA2.90
41Cerebral cavernous malformations 4EnrichmentPIK3CA2.90
42Short syndromeEnrichmentPIK3R12.90
43Hemifacial myohyperplasiaEnrichmentPIK3CA2.90
44Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.90
45Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.90
46Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.90
47Thrombocytopenia 6EnrichmentSRC2.90
48Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.90
49HypospadiasEnrichmentPIK3CA2.90
50Rare venous malformationEnrichmentPIK3CA2.90
51Diaphragmatic eventrationEnrichmentPIK3CA2.90
52Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.90
53Rare combined vascular malformationEnrichmentPIK3CA2.90
54Cavernous lymphangiomaEnrichmentPIK3CA2.90
55Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.90
56Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.90
57Eccrine angiomatous hamartomaEnrichmentPIK3CA2.90
58Egf-related primary hypomagnesemia with intellectual disabilityEnrichmentEGF2.90
59Macrodactyly of toeEnrichmentPIK3CA2.90
60Malignant astrocytomaEnrichmentPTPN112.90
61Lung cancer susceptibility 3EnrichmentEGFR, KRAS2.88
62Lynch syndromeEnrichmentKRAS, PIK3CA2.82
63Immunodeficiency 61EnrichmentSH3KBP12.81
64Deafness, autosomal recessive 39EnrichmentHGF2.81
65Osteofibrous dysplasiaEnrichmentMET2.81
66Deafness, autosomal recessive 97EnrichmentMET2.81
67Autism 9EnrichmentMET2.81
68Arthrogryposis, distal, type 11EnrichmentMET2.81
69Autosomal recessive spastic paraplegia type 59EnrichmentUSP82.81
70Thrombocytopenia 10EnrichmentPTPRJ2.81
71ThrombocytopeniaEnrichmentPTPN11, SRC2.79
72RhabdomyosarcomaEnrichmentCBL, HRAS2.76
73Iga nephropathy 3EnrichmentSPRY22.64
74Takenouchi-kosaki syndromeEnrichmentCDC422.64
75Nocarh syndromeEnrichmentCDC422.64
76Arteriovenous malformations of the brainEnrichmentEGFR, KRAS2.61
77Keratosis, seborrheicEnrichmentPIK3CA2.60
78Noonan syndrome 8EnrichmentPIK3CA2.60
79Werner syndromeEnrichmentPTPN112.60
80Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.60
81Pituitary adenoma 4, acth-secretingEnrichmentUSP82.51
82Ovarian germ cell cancerEnrichmentCBL2.51
83Childhood hepatocellular carcinomaEnrichmentMET2.51
84Papillary renal cell carcinomaEnrichmentMET2.51
85Malignant germ cell tumor of ovaryEnrichmentCBL2.51
86Submucosal cleft palateEnrichmentUBB2.51
87Cleft hard palateEnrichmentUBB2.51
88Breast cancerEnrichmentKRAS, PIK3CA, SHC12.51
89Pompe disease, infantile-onsetEnrichmentPIK3CA2.43
90Neonatal nephrocutaneous inflammatory syndromeEnrichmentEGFR2.43
91Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.43
92Immunodeficiency 14EnrichmentPIK3R12.43
93Tricuspid valve insufficiencyEnrichmentPTPN112.43
94KeratoacanthomaEnrichmentPIK3CA2.43
95Oculoectodermal syndromeEnrichmentKRAS2.41
96Noonan syndrome 4EnrichmentSOS12.41
97Melanosis, neurocutaneousEnrichmentNRAS2.41
98Noonan syndrome 6EnrichmentNRAS2.41
99Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.41
100Cardiofaciocutaneous syndrome 2EnrichmentKRAS2.41
101Alzheimer disease 18EnrichmentADAM102.41
102Reticulate acropigmentation of kitamuraEnrichmentADAM102.41
103Congenital pulmonary airway malformationEnrichmentKRAS2.41
104Phakomatosis pigmentokeratoticaEnrichmentHRAS2.41
105Neurocutaneous melanocytosisEnrichmentNRAS2.41
106Immune system diseaseEnrichmentCDC422.34
107Hydrops fetalis, nonimmuneEnrichmentHRAS, PTPN112.34
108Uvula, bifidEnrichmentUBB2.33
109Cleft soft palateEnrichmentUBB2.33
110Renal cell carcinomaEnrichmentMET2.33
111Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA2.30
112Cerebrovascular diseaseEnrichmentPIK3CA2.30
113Noonan syndrome with multiple lentiginesEnrichmentPTPN112.30
114Familial cerebral cavernous malformationsEnrichmentPIK3CA2.30
115Capillary malformations, congenitalEnrichmentPIK3CA2.20
116LymphomaEnrichmentPTPN112.20
117HemimegalencephalyEnrichmentPIK3CA2.20
118Ovarian cancerEnrichmentEGFR, PIK3CA2.16
119Klippel-trenaunay-weber syndromeEnrichmentPIK3CA2.13
120Hemihyperplasia, isolatedEnrichmentPIK3CA2.13
121Patent ductus arteriosusEnrichmentPTPN112.13
122Myeloproliferative neoplasmEnrichmentCBL2.11
123Aggressive systemic mastocytosisEnrichmentCBL2.11
124Fibromatosis, gingival, 1EnrichmentSOS12.11
125Costello syndromeEnrichmentHRAS2.11
126Pulmonic stenosisEnrichmentSOS12.11
127Encephalocraniocutaneous lipomatosisEnrichmentKRAS2.11
128Inflammatory skin and bowel disease, neonatal, 1EnrichmentADAM172.11
129Wooly hair nevusEnrichmentHRAS2.11
130Rare autosomal recessive non-syndromic sensorineural deafness type dfnbEnrichmentHGF, MET2.08
131MyelofibrosisEnrichmentSRC2.06
132Squamous cell carcinoma, head and neckEnrichmentEGFR2.06
133Overgrowth syndromeEnrichmentPIK3R12.06
134CholangiocarcinomaEnrichmentPTPN32.04
135Renal cell carcinoma, papillary, 1EnrichmentMET1.97
136Oligoarticular juvenile idiopathic arthritisEnrichmentPTPN21.97
137Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentPTPN21.97
138Cowden syndromeEnrichmentPIK3CA1.95
139Inherited cancer-predisposing syndromeEnrichmentEGFR, PTPN111.93
140Nuchal bleb, familialEnrichmentSOS11.93
141Langerhans cell histiocytosisEnrichmentNRAS1.93
142SpermatocytomaEnrichmentHRAS1.93
143Gastric cancerEnrichmentKRAS, PIK3CA1.91
144Arthrogryposis, distal, type 1aEnrichmentMET1.91
145Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.90
146Hereditary breast carcinomaEnrichmentKRAS, PIK3CA1.89
147Pectus excavatumEnrichmentPTPN111.86
148Specific learning disabilityEnrichmentPTPN111.86
149Primary hyperaldosteronismEnrichmentUSP81.86
150EpicanthusEnrichmentPTPN111.83
151MeningiomaEnrichmentPIK3CA1.83
152Congenital long qt syndromeEnrichmentPTPN111.83
153Cardiofaciocutaneous syndrome 1EnrichmentKRAS1.81
154Dowling-degos disease 1EnrichmentADAM101.81
155Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS1.81
156Cardiofaciocutaneous syndromeEnrichmentKRAS1.81
157Lung sarcomatoid carcinomaEnrichmentKRAS1.81
158Pilocytic astrocytomaEnrichmentKRAS1.81
159Epidermolytic nevusEnrichmentHRAS1.81
160Gingival fibromatosisEnrichmentSOS11.81
161OsteoporosisEnrichmentSRC1.76
162Isolated split hand-split foot malformationEnrichmentEPS15L11.74
163GliosarcomaEnrichmentEGFR1.70
164Giant cell glioblastomaEnrichmentEGFR1.68
165Patent foramen ovaleEnrichmentPTPN111.65
166Renal cell carcinoma, nonpapillaryEnrichmentMET1.64
167Endometrial cancerEnrichmentPIK3CA1.58
168Pilomyxoid astrocytomaEnrichmentKRAS1.57
169Hepatocellular carcinomaEnrichmentPIK3CA1.56
170Tooth agenesisEnrichmentTGFA1.56
171ScoliosisEnrichmentPTPN111.53
172StrabismusEnrichmentPTPN111.48
173Prostate cancerEnrichmentPIK3CA1.45
174Long qt syndrome 1EnrichmentPTPN111.43
175Aortic valve disease 1EnrichmentSOS11.30
176Protein-deficiency anemiaEnrichmentNRAS1.30
177Hypertrophic cardiomyopathyEnrichmentPTPN111.28
17846,xy partial gonadal dysgenesisEnrichmentSOS11.27
179Type 2 diabetes mellitusEnrichmentPTPN11.20
180HypertelorismEnrichmentPIK3CA1.20
181Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN111.17
182Sensorineural hearing lossEnrichmentHGF1.14
183Pancreatic cancerEnrichmentKRAS1.03
184Autism spectrum disorderEnrichmentPTPN110.89
185MicrocephalyEnrichmentPTPN110.84
186Hereditary breast ovarian cancer syndromeEnrichmentKRAS0.71
187Myeloma, multipleEnrichmentKRAS0.71

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