Signaling by NTRKs

Pathway network for the Signaling by NTRKs SuperPath

Sources:
  • Reactome

Pathways in the Signaling by NTRKs SuperPath

#NameSourceGenes
1Signaling by NTRKsReactome
2Signaling by NTRK1 (TRKA)Reactome
3Signaling by NTRK3 (TRKC)Reactome
4Retrograde neurotrophin signallingReactome
5PI3K/AKT activationReactome
6Activated NTRK3 signals through RASReactome
7Activated NTRK3 signals through PI3KReactome
8Activation of TRKA receptorsReactome
9NGF-independant TRKA activationReactome
10Activated NTRK3 signals through PLCG1Reactome
11NTF3 activates NTRK3 signalingReactome
12NTRK3 as a dependence receptorReactome

Gene overlap in member pathways for Signaling by NTRKs SuperPath

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

Disorders associated with Signaling by NTRKs SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1RasopathyEnrichmentBRAF, HRAS, KRAS, MAP2K1, MAP2K2, NRAS, PTPN11, RIT1, SOS116.00
2Noonan syndrome and noonan-related syndromeEnrichmentBRAF, HRAS, KRAS, MAP2K1, MAP2K2, NRAS, PTPN11, RIT1, SOS110.82
3Noonan syndrome 1EnrichmentBRAF, HRAS, KRAS, MAP2K1, MAP2K2, NRAS, RIT1, SOS110.69
4Nevus, epidermalEnrichmentHRAS, KRAS, NRAS, PIK3CA10.18
5Lung non-small cell carcinomaEnrichmentBRAF, HRAS, KRAS, MAP2K1, NRAS, PIK3CA9.84
6Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS, KRAS, NRAS9.24
7Differentiated thyroid carcinomaEnrichmentHRAS, KRAS, NRAS, NTRK38.92
8Noonan syndrome 3EnrichmentCLTC, HRAS, KRAS, PTPN11, SOS18.75
9Cardiofaciocutaneous syndrome 1EnrichmentBRAF, KRAS, MAP2K1, MAP2K28.31
10Cardiofaciocutaneous syndromeEnrichmentBRAF, KRAS, MAP2K1, MAP2K28.31
11Ras-associated autoimmune leukoproliferative disorderEnrichmentKRAS, NRAS6.52
12Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R16.31
13Langerhans cell histiocytosisEnrichmentBRAF, MAP2K1, NRAS6.23
14Large congenital melanocytic nevusEnrichmentHRAS, NRAS6.04
15Chronic myelogenous leukemia, bcr-abl1 positiveEnrichmentKRAS, NRAS5.74
16Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA, PIK3R25.63
17Colorectal cancerEnrichmentNRAS, PIK3CA, PIK3R1, SRC5.57
18Neuropathy, hereditary sensory and autonomic, type vEnrichmentNGF, NTRK15.47
19Bladder cancerEnrichmentHRAS, KRAS, PIK3CA5.32
20Hemihyperplasia, isolatedEnrichmentPIK3CA, RHOA5.23
21Thyroid cancer, nonmedullary, 2EnrichmentHRAS, NRAS5.20
22Leukemia, chronic myeloidEnrichmentKRAS, NRAS5.20
23Follicular thyroid carcinomaEnrichmentHRAS, NRAS5.20
24Melanocytic nevus syndrome, congenitalEnrichmentHRAS, NRAS5.07
25Breast adenocarcinomaEnrichmentKRAS, PIK3CA4.71
26Lung squamous cell carcinomaEnrichmentKRAS, PIK3CA4.71
27Juvenile myelomonocytic leukemiaEnrichmentKRAS, NRAS4.70
28Capillary malformation-arteriovenous malformation 1EnrichmentKRAS, MAP2K1, PIK3CA4.69
29Gallbladder cancerEnrichmentBRAF, KRAS, PIK3CA4.69
30Pilomyxoid astrocytomaEnrichmentBRAF, KRAS, NTRK24.69
31Arteriovenous malformationEnrichmentHRAS, PIK3CA4.33
32Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, PIK3CA4.23
33Fibromatosis, gingival, 1EnrichmentREST, SOS14.15
34Pulmonic stenosisEnrichmentBRAF, SOS14.15
35Noonan syndrome 8EnrichmentPIK3CA, RIT14.15
36Lip and oral cavity carcinomaEnrichmentHRAS, PIK3CA4.07
37Breast cancerEnrichmentKRAS, PIK3CA, SHC14.06
38Lynch syndromeEnrichmentKRAS, PIK3CA3.87
39Non-immune hydrops fetalisEnrichmentHRAS, KRAS3.85
40Specific learning disabilityEnrichmentMAPK1, PTPN11, RPS6KA33.84
41Lung cancerEnrichmentBRAF, KRAS, PIK3CA, PPP2R1B3.83
42Melanoma of soft tissueEnrichmentATF1, CREB13.67
43Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG13.66
44Leukemia, acute myeloidEnrichmentKRAS, NRAS3.63
45Congenital mesoblastic nephromaEnrichmentNTRK33.53
46FibrosarcomaEnrichmentNTRK33.53
47Type 2 diabetes mellitusEnrichmentIRS1, IRS23.48
48Developmental and epileptic encephalopathy 58EnrichmentNTRK23.43
49Obesity, hyperphagia, and developmental delayEnrichmentNTRK23.43
50Acute encephalopathy with biphasic seizures and late reduced diffusionEnrichmentADORA2A3.43
51Chromosome 22q11.2 deletion syndrome, distalEnrichmentCRKL, MAPK13.37
52Gingival fibromatosisEnrichmentREST, SOS13.37
53MacrodactylyEnrichmentPIK3CA3.35
54Megalencephaly, autosomal dominantEnrichmentPIK3CA3.35
55Cowden syndrome 5EnrichmentPIK3CA3.35
56Cerebral cavernous malformations 4EnrichmentPIK3CA3.35
57Short syndromeEnrichmentPIK3R13.35
58Hemifacial myohyperplasiaEnrichmentPIK3CA3.35
59Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA3.35
60Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R13.35
61Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R13.35
62Thrombocytopenia 6EnrichmentSRC3.35
63Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA3.35
64HypospadiasEnrichmentPIK3CA3.35
65Rare venous malformationEnrichmentPIK3CA3.35
66Diaphragmatic eventrationEnrichmentPIK3CA3.35
67Pik3ca-related overgrowth spectrumEnrichmentPIK3CA3.35
68Rare combined vascular malformationEnrichmentPIK3CA3.35
69Cavernous lymphangiomaEnrichmentPIK3CA3.35
70Pik3ca-related overgrowth syndromeEnrichmentPIK3CA3.35
71Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA3.35
72Eccrine angiomatous hamartomaEnrichmentPIK3CA3.35
73Macrodactyly of toeEnrichmentPIK3CA3.35
74Noonan syndrome with multiple lentiginesEnrichmentBRAF, PTPN113.25
75GliomaEnrichmentNTRK33.23
76Oculoectodermal syndromeEnrichmentKRAS3.23
77Noonan syndrome 4EnrichmentSOS13.23
78Melanosis, neurocutaneousEnrichmentNRAS3.23
79Noonan syndrome 6EnrichmentNRAS3.23
80Cardiofaciocutaneous syndrome 2EnrichmentKRAS3.23
81Congenital pulmonary airway malformationEnrichmentKRAS3.23
82Phakomatosis pigmentokeratoticaEnrichmentHRAS3.23
83Neurocutaneous melanocytosisEnrichmentNRAS3.23
84Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomaliesEnrichmentRHOA3.18
85Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomaliesEnrichmentRHOA3.18
86Histiocytoid hemangiomaEnrichmentFOS, FOSB3.15
87Insensitivity to pain, congenital, with anhidrosisEnrichmentNTRK13.13
88Pain sensitivity quantitative trait locus 1EnrichmentNTRK13.13
89Keratosis, seborrheicEnrichmentPIK3CA3.05
90Rosette-forming glioneuronal tumorEnrichmentPIK3CA3.05
91Hypocalciuric hypercalcemia, familial, type iiiEnrichmentAP2S12.99
92Charcot-marie-tooth disease, dominant intermediate bEnrichmentDNM22.99
93Mirror movements 3EnrichmentDNAL42.99
94Lethal congenital contracture syndrome 5EnrichmentDNM22.99
95Autosomal dominant charcot-marie-tooth disease type 2mEnrichmentDNM22.99
96Thyroid carcinoma, familial medullaryEnrichmentNTRK12.96
97Gastric cancerEnrichmentKRAS, PIK3CA2.94
98Costello syndromeEnrichmentHRAS2.93
99Encephalocraniocutaneous lipomatosisEnrichmentKRAS2.93
100Wooly hair nevusEnrichmentHRAS2.93
101Nephrotic syndrome, type 6EnrichmentPTPRO2.93
102Hereditary breast carcinomaEnrichmentKRAS, PIK3CA2.92
103Myeloma, multipleEnrichmentBRAF, KRAS, PIK3R2, SGK12.89
104Pompe disease, infantile-onsetEnrichmentPIK3CA2.88
105Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.88
106Immunodeficiency 14EnrichmentPIK3R12.88
107KeratoacanthomaEnrichmentPIK3CA2.88
108Undetermined early-onset epileptic encephalopathyEnrichmentCLTC, DNM12.83
109Cerebrovascular diseaseEnrichmentPIK3CA2.75
110Familial cerebral cavernous malformationsEnrichmentPIK3CA2.75
111Nuchal bleb, familialEnrichmentSOS12.75
112SpermatocytomaEnrichmentHRAS2.75
113Ovarian cancerEnrichmentNTRK1, PIK3CA2.72
114Hydrops fetalis, nonimmuneEnrichmentHRAS, PTPN11, RIT12.69
115Intellectual developmental disorder, autosomal dominant 60, with seizuresEnrichmentAP2M12.69
116Capillary malformations, congenitalEnrichmentPIK3CA2.66
117HemimegalencephalyEnrichmentPIK3CA2.66
118Diffuse gastric and lobular breast cancer syndromeEnrichmentKRAS2.63
119Lung sarcomatoid carcinomaEnrichmentKRAS2.63
120Pilocytic astrocytomaEnrichmentKRAS2.63
121Epidermolytic nevusEnrichmentHRAS2.63
122Ventricular septal defectEnrichmentBRAF, RPS6KA32.61
123Klippel-trenaunay-weber syndromeEnrichmentPIK3CA2.58
124Cowden syndrome 1EnrichmentPIK3CA2.58
125Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R22.58
126MyelofibrosisEnrichmentSRC2.51
127Overgrowth syndromeEnrichmentPIK3R12.51
128Myopathy, centronuclear, x-linkedEnrichmentDNM22.51
129Intellectual developmental disorder, autosomal dominant 56EnrichmentCLTC2.51
130Developmental and epileptic encephalopathy 31bEnrichmentDNM12.51
131Adult hepatocellular carcinomaEnrichmentPIK3CA2.40
132Cowden syndromeEnrichmentPIK3CA2.40
133Mirror movements 1EnrichmentDNAL42.38
134Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1EnrichmentCLTC2.38
135Autism spectrum disorderEnrichmentGRIN2B, MAP2K1, MEF2C, PTPN11, TCF122.36
136Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R12.35
137Developmental and epileptic encephalopathy 31aEnrichmentDNM12.29
138MeningiomaEnrichmentPIK3CA2.28
139Lung cancer susceptibility 3EnrichmentBRAF, KRAS2.22
140Myopathy, centronuclear, 1EnrichmentDNM22.21
141Inflammatory myofibroblastic tumorEnrichmentCLTC2.21
142OsteoporosisEnrichmentSRC2.21
143Nk-cell enteropathyEnrichmentPIK3CB, PTPRS2.16
144Wilms tumor 1EnrichmentBRAF, REST2.16
145Renal cell carcinoma with mit translocationsEnrichmentCLTC2.14
146Complex neurodevelopmental disorderEnrichmentDOCK3, GRIN2B, PPP2CA, RALA, TIAM12.13
147Aortic valve disease 1EnrichmentSOS12.12
148Protein-deficiency anemiaEnrichmentNRAS2.12
149Lennox-gastaut syndromeEnrichmentDNM12.08
15046,xy partial gonadal dysgenesisEnrichmentSOS12.08
151Coffin-lowry syndromeEnrichmentRPS6KA32.07
152Charcot-marie-tooth disease, demyelinating, type 1dEnrichmentEGR22.07
153Melorheostosis, isolatedEnrichmentMAP2K12.07
154Noonan syndrome 7EnrichmentBRAF2.07
155Leopard syndrome 3EnrichmentBRAF2.07
156Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.07
157Lissencephaly 7 with cerebellar hypoplasiaEnrichmentCDK52.07
158Wilms tumor 6EnrichmentREST2.07
159Hiatt-neu-cooper neurodevelopmental syndromeEnrichmentRALA2.07
160Ventriculomegaly and arthrogryposisEnrichmentKIDINS2202.07
161Noonan syndrome 13EnrichmentMAPK12.07
162Intellectual developmental disorder, x-linked 19EnrichmentRPS6KA32.07
163T-cell large granular lymphocyte leukemiaEnrichmentSTAT32.07
164Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired languageEnrichmentMEF2C2.07
165Houge-janssens syndrome 2EnrichmentPPP2R1A2.07
166LymphangiomaEnrichmentBRAF2.07
167Coronary artery disease, autosomal dominant, 1EnrichmentMEF2A2.07
168Phace associationEnrichmentBRAF2.07
169MelorheostosisEnrichmentMAP2K12.07
170Deafness, autosomal dominant 27EnrichmentREST2.07
171Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.07
172Craniosynostosis 3EnrichmentTCF122.07
173Hypogonadotropic hypogonadism 19 with or without anosmiaEnrichmentDUSP62.07
174Macular dystrophy, patterned, 3EnrichmentMAPKAPK32.07
175Fibromatosis, gingival, 5EnrichmentREST2.07
176Autoimmune disease, multisystem, infantile-onset, 1EnrichmentSTAT32.07
177Symptomatic form of coffin-lowry syndrome in female carriersEnrichmentRPS6KA32.07
178Charcot-marie-tooth disease type 1dEnrichmentEGR22.07
179Stat3-related early-onset multisystem autoimmune diseaseEnrichmentSTAT32.07
1805q14.3 microdeletion syndromeEnrichmentMEF2C2.07
181Complete atrioventricular septal defect without ventricular hypoplasiaEnrichmentMEF2C2.07
182Syringocystadenoma papilliferumEnrichmentBRAF2.07
183GangliogliomaEnrichmentBRAF2.07
184Hypogonadotropic hypogonadism 26 with or without anosmiaEnrichmentTCF122.07
185Nongerminomatous germ cell tumorEnrichmentBRAF2.07
186Phace syndromeEnrichmentBRAF2.07
187Mef2c-related disorderEnrichmentMEF2C2.07
188Ppp2r1a-related neurodevelopmental disorderEnrichmentPPP2R1A2.07
189Classic hairy cell leukemiaEnrichmentBRAF2.07
190Chronic lymphoproliferative disorder of natural killer cellsEnrichmentSTAT32.07
191West syndromeEnrichmentDNM1, GRIN2B, NTRK22.04
192Myoclonic-atonic epilepsyEnrichmentAP2M12.03
193Endometrial cancerEnrichmentPIK3CA2.03
194RhabdomyosarcomaEnrichmentHRAS2.03
195Hepatocellular carcinomaEnrichmentPIK3CA2.01
196HypertelorismEnrichmentPIK3CA, RIT1, RPS6KA32.01
197MetachondromatosisEnrichmentPTPN112.01
198Deafness, autosomal recessive 26EnrichmentGAB12.01
199Leopard syndrome 1EnrichmentPTPN112.01
200Developmental and epileptic encephalopathy 27EnrichmentGRIN2B2.01
201Intellectual developmental disorder, autosomal dominant 6, with or without seizuresEnrichmentGRIN2B2.01
202Glaucoma 1, open angle, oEnrichmentNTF42.01
203Neurodevelopmental disorder with language delay and seizuresEnrichmentTIAM12.01
204Neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxiaEnrichmentDOCK32.01
205Grin2b-related neurodevelopmental disorderEnrichmentGRIN2B2.01
206Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.01
207Malignant astrocytomaEnrichmentPTPN112.01
208Arteriovenous malformations of the brainEnrichmentBRAF, KRAS1.96
209Diffuse large b-cell lymphomaEnrichmentBRAF, STAT31.96
210Prostate cancerEnrichmentPIK3CA1.89
211Stereotypic movement disorderEnrichmentDNM11.87
212Peripheral nervous system diseaseEnrichmentNGF1.85
213NeuropathyEnrichmentNGF1.85
214Pancreatic cancerEnrichmentKRAS1.83
215CraniosynostosisEnrichmentGRIN2B, TCF121.79
216Scoliosis, isolated 1EnrichmentMAPK71.77
217Hemangiopericytoma, malignantEnrichmentNAB21.77
218Histiocytoma, angiomatoid fibrousEnrichmentCREB11.77
219Neuropathy, congenital hypomyelinating, 1, autosomal recessiveEnrichmentEGR21.77
220Sifrim-hitz-weiss syndromeEnrichmentCHD41.77
221Spastic paraplegia, intellectual disability, nystagmus, and obesityEnrichmentKIDINS2201.77
222Houge-janssens syndrome 1EnrichmentPPP2R5D1.77
223Menke-hennekam syndrome 2EnrichmentEP3001.77
224Houge-janssens syndrome 3EnrichmentPPP2CA1.77
225Tafro syndromeEnrichmentMAP2K21.77
226Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC11.71
227Werner syndromeEnrichmentPTPN111.71
228ThrombocytopeniaEnrichmentSRC1.68
229Centronuclear myopathyEnrichmentDNM21.67
230Primary ovarian insufficiencyEnrichmentNTRK11.67
231ScoliosisEnrichmentGRIN2B, PTPN111.64
232Hyper-ige syndrome 1, autosomal dominant, with recurrent infectionsEnrichmentSTAT31.60
233Ataxia-telangiectasiaEnrichmentBRAF1.60
234Tethered spinal cord syndromeEnrichmentBRAF1.60
235Bacteremia 2EnrichmentMAPKAPK31.60
236Breast implant-associated anaplastic large cell lymphomaEnrichmentSTAT31.60
237Hyper ige syndromeEnrichmentSTAT31.60
238Charcot-marie-tooth disease type 1EnrichmentEGR21.60
239Tricuspid valve insufficiencyEnrichmentPTPN111.54
240Hereditary breast ovarian cancer syndromeEnrichmentKRAS1.50
241MicrocephalyEnrichmentEP300, GRIN2B, MAPK1, PTPN111.48
242Thyroid cancer, nonmedullary, 1EnrichmentBRAF1.48
243Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.48
244Congenital generalized lipodystrophyEnrichmentFOS1.48
245CraniopharyngiomaEnrichmentBRAF1.48
246TuberculosisEnrichmentMAPKAPK31.48
247Newborn respiratory distress syndromeEnrichmentBRAF1.48
248Non-syndromic bicoronal craniosynostosisEnrichmentTCF121.48
249Haddad syndromeEnrichmentASCL11.48
250Pseudomyogenic hemangioendotheliomaEnrichmentFOSB1.48
251AstigmatismEnrichmentGRIN2B1.41
252Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentPTPN111.41
253Genetic steroid-resistant nephrotic syndromeEnrichmentPTPRO1.40
254MyopathyEnrichmentDNM21.39
255Charcot-marie-tooth diseaseEnrichmentDNM21.38
256Hypertrophic neuropathy of dejerine-sottasEnrichmentEGR21.38
257Chondrosarcoma, extraskeletal myxoidEnrichmentTCF121.38
258Rubinstein-taybi syndrome 2EnrichmentEP3001.38
259LymphomaEnrichmentPTPN111.32
260Sleep disorderEnrichmentGRIN2B1.32
261Kabuki syndrome 1EnrichmentKIDINS2201.30
262Rubinstein-taybi syndrome 1EnrichmentEP3001.30
263Wilms tumor 5EnrichmentBRAF1.30
264Chromosome 16p13.3 deletion syndrome, proximalEnrichmentEP3001.30
265Autosomal dominant non-syndromic intellectual disabilityEnrichmentCLTC1.30
266Cerebral palsyEnrichmentGRIN2B, KIDINS2201.25
267Wilms tumor, aniridia, genitourinary anomalies, and impaired intellectual development syndromeEnrichmentBDNF1.24
268Patent ductus arteriosusEnrichmentPTPN111.24
269Gastroesophageal refluxEnrichmentRPS6KA31.18
270Lymphoma, non-hodgkin, familialEnrichmentBRAF1.18
271Orthostatic intoleranceEnrichmentRPS6KA31.18
272Permanent neonatal diabetes mellitusEnrichmentSTAT31.18
273Cardiomyopathy, familial hypertrophic, 4EnrichmentBRAF1.13
274Charge syndromeEnrichmentEP3001.13
275Primary hyperaldosteronismEnrichmentBRAF1.13
276MelanomaEnrichmentBRAF1.09
277Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.07
278Congenital central hypoventilation syndromeEnrichmentBDNF1.07
279Pectus excavatumEnrichmentPTPN110.99
280Acute promyelocytic leukemiaEnrichmentSTAT30.98
281EpicanthusEnrichmentPTPN110.95
282Congenital long qt syndromeEnrichmentPTPN110.95
283Heart diseaseEnrichmentRIT10.95
284Polydactyly, postaxial, type a1EnrichmentEP3000.92
285Rare genetic intellectual disabilityEnrichmentEP3000.92
286Melanoma, cutaneous malignant 1EnrichmentBRAF0.87
287Dandy-walker syndromeEnrichmentBRAF0.87
288Heart, malformation ofEnrichmentMAPK10.85
289Charcot-marie-tooth disease type 4EnrichmentEGR20.85
290Normosmic congenital hypogonadotropic hypogonadismEnrichmentDUSP60.85
291Patent foramen ovaleEnrichmentPTPN110.79
292MalariaEnrichmentMAPKAPK30.75
293Kallmann syndromeEnrichmentDUSP60.75
294StrabismusEnrichmentPTPN110.63
295Long qt syndrome 1EnrichmentPTPN110.59
296Non-syndromic x-linked intellectual disabilityEnrichmentRPS6KA30.58
297EpilepsyEnrichmentGRIN2B0.49
298Hypertrophic cardiomyopathyEnrichmentPTPN110.46
299Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentREST0.45
300Body mass index quantitative trait locus 11EnrichmentBDNF0.41
301Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentMEF2C0.41
302Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.37
303Dilated cardiomyopathyEnrichmentBRAF0.31
304Inherited cancer-predisposing syndromeEnrichmentPTPN110.14

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