RET signaling

No Pathway Network information available for RET signaling

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

Disorders associated with RET signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Noonan syndrome 3EnrichmentHRAS, PTPN11, SOS16.15
2Arteriovenous malformationEnrichmentHRAS, PIK3CA, RASA15.77
3Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, PIK3CA, RASA15.62
4Noonan syndrome and noonan-related syndromeEnrichmentHRAS, PTPN11, SOS15.04
5Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R14.64
6Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3CD, PIK3R14.60
7Immunodeficiency 14EnrichmentPIK3CD, PIK3R14.60
8Noonan syndrome 1EnrichmentHRAS, PTPN11, SOS14.46
9RasopathyEnrichmentHRAS, PTPN11, SOS14.30
10Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA, PIK3R24.30
11Breast cancerEnrichmentJUN, PIK3CA, RET, SHC14.26
12Capillary malformations, congenitalEnrichmentPIK3CA, RASA14.12
13Hirschsprung disease 1EnrichmentGDNF, NRTN, RET4.08
14Colorectal cancerEnrichmentPIK3CA, PIK3R1, RET, SRC4.01
15Klippel-trenaunay-weber syndromeEnrichmentPIK3CA, RASA13.94
16Hemihyperplasia, isolatedEnrichmentPIK3CA, RHOA3.94
17Nevus, epidermalEnrichmentHRAS, PIK3CA3.80
18Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA, RASA13.80
19Congenital central hypoventilation syndromeEnrichmentGDNF, RET3.57
20Renal agenesis, bilateralEnrichmentGFRA1, RET3.57
21Ellis-van creveld syndromeEnrichmentPRKACA, PRKACB3.52
22Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3CD, PIK3R13.42
23Lung non-small cell carcinomaEnrichmentHRAS, PIK3CA3.38
24Lip and oral cavity carcinomaEnrichmentHRAS, PIK3CA3.30
25Hepatocellular carcinomaEnrichmentPIK3CA, RET2.77
26Hydrops fetalis, nonimmuneEnrichmentHRAS, PTPN112.62
27Multiple endocrine neoplasia, type iibEnrichmentRET2.55
28MacrodactylyEnrichmentPIK3CA2.55
29MetachondromatosisEnrichmentPTPN112.55
30Cystic angiomatosis of bone, diffuseEnrichmentRASA12.55
31Deafness, autosomal recessive 26EnrichmentGAB12.55
32Noonan syndrome 4EnrichmentSOS12.55
33Megalencephaly, autosomal dominantEnrichmentPIK3CA2.55
34Leopard syndrome 1EnrichmentPTPN112.55
35Cowden syndrome 5EnrichmentPIK3CA2.55
36Cerebral cavernous malformations 4EnrichmentPIK3CA2.55
37Short syndromeEnrichmentPIK3R12.55
38Renal hypodysplasia/aplasia 4EnrichmentGFRA12.55
39Hemifacial myohyperplasiaEnrichmentPIK3CA2.55
40Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.55
41Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.55
42Pigmented nodular adrenocortical disease, primary, 4EnrichmentPRKACA2.55
43Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.55
44Hirschsprung disease 3EnrichmentGDNF2.55
45Schizophrenia 15EnrichmentSHANK32.55
46Cardioacrofacial dysplasia 1EnrichmentPRKACA2.55
47Thrombocytopenia 6EnrichmentSRC2.55
48Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomaliesEnrichmentRHOA2.55
49Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomaliesEnrichmentRHOA2.55
50Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.55
51HypospadiasEnrichmentPIK3CA2.55
52Thyroid cancerEnrichmentRET2.55
53MutismEnrichmentSHANK32.55
54Rare venous malformationEnrichmentPIK3CA2.55
55Gorham's diseaseEnrichmentRASA12.55
56Diaphragmatic eventrationEnrichmentPIK3CA2.55
57Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.55
58Rare combined vascular malformationEnrichmentPIK3CA2.55
59Cavernous lymphangiomaEnrichmentPIK3CA2.55
60Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.55
61Phakomatosis pigmentokeratoticaEnrichmentHRAS2.55
62Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.55
63Silver-russell syndrome due to maternal uniparental disomy of chromosome 7EnrichmentGRB102.55
64Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.55
65Eccrine angiomatous hamartomaEnrichmentPIK3CA2.55
66Macrodactyly of toeEnrichmentPIK3CA2.55
67Gastrointestinal system diseaseEnrichmentRET2.55
68Malignant astrocytomaEnrichmentPTPN112.55
69Multiple endocrine neoplasiaEnrichmentRET2.55
70Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.53
71Cardioacrofacial dysplasia 2EnrichmentPRKACB2.53
72Immunodeficiency 14b, autosomal recessiveEnrichmentPIK3CD2.53
73Bladder cancerEnrichmentHRAS, PIK3CA2.53
74Differentiated thyroid carcinomaEnrichmentHRAS, RET2.53
75Non-immune hydrops fetalisEnrichmentHRAS, PTPN112.47
76Fibromatosis, gingival, 1EnrichmentSOS12.25
77Costello syndromeEnrichmentHRAS2.25
78Pulmonic stenosisEnrichmentSOS12.25
79Histiocytoma, angiomatoid fibrousEnrichmentCREB12.25
80Keratosis, seborrheicEnrichmentPIK3CA2.25
81Noonan syndrome 8EnrichmentPIK3CA2.25
82Myopia 28, autosomal recessiveEnrichmentDOK12.25
83Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.25
84Werner syndromeEnrichmentPTPN112.25
85Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.25
86Phelan-mcdermid syndromeEnrichmentSHANK32.25
87Medullary thyroid carcinomaEnrichmentRET2.25
88Fibrolamellar carcinomaEnrichmentPRKACA2.25
89Psychotic disorderEnrichmentSHANK32.25
90Wooly hair nevusEnrichmentHRAS2.25
91Scoliosis, isolated 1EnrichmentMAPK72.23
92Roifman-chitayat syndromeEnrichmentPIK3CD2.23
93Bleeding disorder, platelet-type, 19EnrichmentPRKACG2.23
94Immune system diseaseEnrichmentPIK3CD2.23
95Type 2 diabetes mellitusEnrichmentIRS1, IRS22.21
96Hereditary breast carcinomaEnrichmentPIK3CA, RET2.17
97ThrombocytopeniaEnrichmentPTPN11, SRC2.10
98Thyroid carcinoma, familial medullaryEnrichmentRET2.08
99Pompe disease, infantile-onsetEnrichmentPIK3CA2.08
100Nuchal bleb, familialEnrichmentSOS12.08
101Large congenital melanocytic nevusEnrichmentHRAS2.08
102Wieacker-wolff syndromeEnrichmentRASA12.08
103Gingival overgrowthEnrichmentRET2.08
104SpermatocytomaEnrichmentHRAS2.08
105Melanoma of soft tissueEnrichmentCREB12.08
106Tricuspid valve insufficiencyEnrichmentPTPN112.08
107KeratoacanthomaEnrichmentPIK3CA2.08
108HypertelorismEnrichmentPIK3CA, RET2.03
109Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS1.95
110Central hypoventilation syndrome, congenital, 1EnrichmentRET1.95
111Cerebrovascular diseaseEnrichmentPIK3CA1.95
112Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN111.95
113Noonan syndrome with multiple lentiginesEnrichmentPTPN111.95
114Epidermolytic nevusEnrichmentHRAS1.95
115Familial cerebral cavernous malformationsEnrichmentPIK3CA1.95
116Haddad syndromeEnrichmentRET1.95
117Gingival fibromatosisEnrichmentSOS11.95
118Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R21.93
119Multiple endocrine neoplasia, type iiaEnrichmentRET1.86
120LymphomaEnrichmentPTPN111.86
121HemimegalencephalyEnrichmentPIK3CA1.86
122Cowden syndrome 1EnrichmentPIK3CA1.78
123Telangiectasia, hereditary hemorrhagic, type 1EnrichmentRASA11.78
124Hemangioma, capillary infantileEnrichmentRASA11.78
125Basal cell carcinoma 1EnrichmentRASA11.78
126Patent ductus arteriosusEnrichmentPTPN111.78
127Breast adenocarcinomaEnrichmentPIK3CA1.78
128Lung squamous cell carcinomaEnrichmentPIK3CA1.78
129Sporadic pheochromocytoma/secreting paragangliomaEnrichmentRET1.78
130Thyroid cancer, nonmedullary, 2EnrichmentHRAS1.71
131MyelofibrosisEnrichmentSRC1.71
132Gallbladder cancerEnrichmentPIK3CA1.71
133Hereditary hemorrhagic telangiectasiaEnrichmentRASA11.71
134Follicular thyroid carcinomaEnrichmentHRAS1.71
135Overgrowth syndromeEnrichmentPIK3R11.71
136Melanocytic nevus syndrome, congenitalEnrichmentHRAS1.65
137Renal hypodysplasia/aplasia 1EnrichmentRET1.65
138HypothyroidismEnrichmentRET1.65
139Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.60
140Adult hepatocellular carcinomaEnrichmentPIK3CA1.60
141Cowden syndromeEnrichmentPIK3CA1.60
142Pectus excavatumEnrichmentPTPN111.52
143Specific learning disabilityEnrichmentPTPN111.52
144Ovarian cancerEnrichmentPIK3CA, RET1.49
145EpicanthusEnrichmentPTPN111.48
146Juvenile myelomonocytic leukemiaEnrichmentPTPN111.48
147Renal hypodysplasia/aplasia 3EnrichmentRET1.48
148MeningiomaEnrichmentPIK3CA1.48
149Congenital long qt syndromeEnrichmentPTPN111.48
150Aortic valve disease 1EnrichmentSOS11.45
151Autism spectrum disorderEnrichmentPTPN11, SHANK31.43
152Nk-cell enteropathyEnrichmentPIK3CB1.42
153OsteoporosisEnrichmentSRC1.41
154PheochromocytomaEnrichmentRET1.41
15546,xy partial gonadal dysgenesisEnrichmentSOS11.41
156Lynch syndromeEnrichmentPIK3CA1.38
157RhabdomyosarcomaEnrichmentHRAS1.36
158Patent foramen ovaleEnrichmentPTPN111.31
159Inherited cancer-predisposing syndromeEnrichmentPTPN11, RET1.28
160Endometrial cancerEnrichmentPIK3CA1.24
161Hereditary paraganglioma-pheochromocytoma syndromesEnrichmentRET1.24
162ScoliosisEnrichmentPTPN111.19
163Tetralogy of fallotEnrichmentRET1.15
164StrabismusEnrichmentPTPN111.14
165Prostate cancerEnrichmentPIK3CA1.11
166Long qt syndrome 1EnrichmentPTPN111.09
167Lung cancerEnrichmentPIK3CA1.07
168Gastric cancerEnrichmentPIK3CA0.94
169Hypertrophic cardiomyopathyEnrichmentPTPN110.94
170Sensorineural hearing lossEnrichmentRET0.90
171Hereditary breast ovarian cancer syndromeEnrichmentBCAR10.84
172Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.84
173Myeloma, multipleEnrichmentPIK3R20.82
174MicrocephalyEnrichmentPTPN110.53

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