Immune response Fc epsilon RI pathway

Pathway network for the Immune response Fc epsilon RI pathway SuperPath

Sources:
  • GeneGo (Thomson Reuters)
  • PubChem

Pathways in the Immune response Fc epsilon RI pathway SuperPath

Gene overlap in member pathways for Immune response Fc epsilon RI pathway SuperPath

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

Disorders associated with Immune response Fc epsilon RI pathway SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1RasopathyEnrichmentCBL, HRAS, MAP2K1, MAP2K2, PTPN11, RAF1, SOS116.00
2Autosomal non-syndromic agammaglobulinemiaEnrichmentBLNK, CD79A, CD79B, IGHM, PIK3CD, PIK3R111.87
3Noonan syndrome and noonan-related syndromeEnrichmentCBL, HRAS, MAP2K1, MAP2K2, PTPN11, RAF1, SOS111.63
4Noonan syndrome 1EnrichmentCBL, HRAS, MAP2K1, MAP2K2, PTPN11, RAF1, SOS110.60
5Noonan syndrome 3EnrichmentHRAS, PTPN11, RAF1, SOS17.89
6Arteriovenous malformationEnrichmentHRAS, MAP2K1, PIK3CA, RASA17.34
7Myopathy, x-linked, with excessive autophagyEnrichmentHRAS, MAP2K1, PIK3CA, RASA17.12
8Agammaglobulinemia 1, autosomal recessiveEnrichmentBTK, IGH, IGHM6.86
9Agammaglobulinemia 1EnrichmentBTK, IGH, IGHM6.86
10Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentAKT3, PIK3CA, PIK3R26.26
11HemimegalencephalyEnrichmentAKT3, PIK3CA, PTEN5.87
12Capillary malformation-arteriovenous malformation 1EnrichmentMAP2K1, PIK3CA, RASA15.52
13Catecholaminergic polymorphic ventricular tachycardiaEnrichmentCALM1, CALM2, CALM35.12
14Cowden syndromeEnrichmentAKT1, PIK3CA, PTEN4.95
15Lung non-small cell carcinomaEnrichmentHRAS, MAP2K1, PIK3CA4.86
16Long qt syndrome 1EnrichmentCALM1, CALM2, CALM3, ITPR34.77
17Immunoglobulin kappa light chain deficiencyEnrichmentIGK, IGKC4.57
18Immune system diseaseEnrichmentCDC42, PIK3CD4.57
19Common variable immunodeficiency phenotype due to cd19/cd81 deficiencyEnrichmentCD19, CD814.57
20MeningiomaEnrichmentAKT1, PIK3CA, PTEN4.53
21Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG, NFKBIA4.43
22Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R14.23
23Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3CD, PIK3R14.09
24Immunodeficiency 14EnrichmentPIK3CD, PIK3R14.09
25Recurrent infections associated with rare immunoglobulin isotypes deficiencyEnrichmentIGK, IGKC4.09
26Cardiofaciocutaneous syndrome 1EnrichmentMAP2K1, MAP2K23.93
27Cardiofaciocutaneous syndromeEnrichmentMAP2K1, MAP2K23.93
28Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCBL, PTPN113.93
29Noonan syndrome with multiple lentiginesEnrichmentPTPN11, RAF13.93
30Diffuse large b-cell lymphomaEnrichmentBTK, CD79B, PTEN3.90
31Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentAKT3, PIK3R23.79
32Capillary malformations, congenitalEnrichmentPIK3CA, RASA13.71
33Follicular lymphomaEnrichmentBCL6, IGH3.57
34Klippel-trenaunay-weber syndromeEnrichmentPIK3CA, RASA13.53
35Breast adenocarcinomaEnrichmentAKT1, PIK3CA3.53
36Breast cancerEnrichmentAKT1, JUN, PIK3CA, SHC13.45
37Cowden syndrome 1EnrichmentPIK3CA, PTEN3.40
38Nevus, epidermalEnrichmentHRAS, PIK3CA3.39
39Bladder cancerEnrichmentHRAS, PIK3CA, PTEN3.34
40Melanocytic nevus syndrome, congenitalEnrichmentHRAS, RAF13.26
41Thyroid cancer, nonmedullary, 2EnrichmentHRAS, PTEN3.25
42Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.25
43Follicular thyroid carcinomaEnrichmentHRAS, PTEN3.25
44Specific learning disabilityEnrichmentMAPK1, PTPN112.97
45Juvenile myelomonocytic leukemiaEnrichmentCBL, PTPN112.89
46Lip and oral cavity carcinomaEnrichmentHRAS, PIK3CA2.89
47Hereditary breast carcinomaEnrichmentAKT1, PIK3CA, PTEN2.81
4846,xy partial gonadal dysgenesisEnrichmentMAP3K1, SOS12.76
49RhabdomyosarcomaEnrichmentCBL, HRAS2.64
50MacrodactylyEnrichmentPIK3CA2.35
51Proteus syndromeEnrichmentAKT12.35
52MetachondromatosisEnrichmentPTPN112.35
53Cystic angiomatosis of bone, diffuseEnrichmentRASA12.35
54Incontinentia pigmentiEnrichmentIKBKG2.35
55Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.35
56Noonan syndrome 5EnrichmentRAF12.35
57Noonan syndrome 4EnrichmentSOS12.35
58Melorheostosis, isolatedEnrichmentMAP2K12.35
59Megalencephaly, autosomal dominantEnrichmentPIK3CA2.35
60Leopard syndrome 1EnrichmentPTPN112.35
61Cardiomyopathy, dilated, 1nnEnrichmentRAF12.35
62Cowden syndrome 5EnrichmentPIK3CA2.35
63Cardiofaciocutaneous syndrome 3EnrichmentMAP2K12.35
64Fetal encasement syndromeEnrichmentCHUK2.35
65Wiskott-aldrich syndrome 2EnrichmentWIPF12.35
6646,xy sex reversal 6EnrichmentMAP3K12.35
67Cerebral cavernous malformations 4EnrichmentPIK3CA2.35
68Immunodeficiency 15bEnrichmentIKBKB2.35
69Noonan syndrome 13EnrichmentMAPK12.35
70Immunodeficiency 81EnrichmentLCP22.35
71Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.35
72Immunodeficiency 15aEnrichmentIKBKB2.35
73Knobloch syndrome 2EnrichmentPAK22.35
74Short syndromeEnrichmentPIK3R12.35
75Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.35
76Developmental and epileptic encephalopathy 89EnrichmentGAD12.35
77Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.35
78Isolated growth hormone deficiency type iiiEnrichmentBTK2.35
79Hemifacial myohyperplasiaEnrichmentPIK3CA2.35
80Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.35
81Lymphoproliferative syndrome 1EnrichmentITK2.35
82MelorheostosisEnrichmentMAP2K12.35
83Leopard syndrome 2EnrichmentRAF12.35
84Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorderEnrichmentPLA2G4A2.35
85Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.35
86Cardiofaciocutaneous syndrome 4EnrichmentMAP2K22.35
87Cowden syndrome 6EnrichmentAKT12.35
88Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.35
89Gastrointestinal ulceration, recurrent, with dysfunctional plateletsEnrichmentPLA2G4A2.35
90Bartsocas-papas syndrome 2EnrichmentCHUK2.35
91Autoinflammatory disease, systemic, with vasculitisEnrichmentLYN2.35
92TrigonitisEnrichmentRAF12.35
93Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.35
94HypospadiasEnrichmentPIK3CA2.35
95ColitisEnrichmentSYK2.35
96Rare venous malformationEnrichmentPIK3CA2.35
97Gorham's diseaseEnrichmentRASA12.35
98Diaphragmatic eventrationEnrichmentPIK3CA2.35
99Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.35
100Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.35
101Rare combined vascular malformationEnrichmentPIK3CA2.35
102Cavernous lymphangiomaEnrichmentPIK3CA2.35
103Cryptogenic multifocal ulcerous stenosing enteritisEnrichmentPLA2G4A2.35
104Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.35
105Phakomatosis pigmentokeratoticaEnrichmentHRAS2.35
106Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.35
107Eccrine angiomatous hamartomaEnrichmentPIK3CA2.35
108Macrodactyly of toeEnrichmentPIK3CA2.35
109Malignant astrocytomaEnrichmentPTPN112.35
110MalariaEnrichmentFCGR2B, IKBKG2.32
111Anhidrosis, isolated, with normal sweat glandsEnrichmentITPR22.28
112Hypoinsulinemic hypoglycemia with hemihypertrophyEnrichmentAKT22.28
113Vacterl association with hydrocephalusEnrichmentPTEN2.28
114Noonan syndrome 9EnrichmentSOS22.28
115Immunodeficiency, common variable, 6EnrichmentCD812.28
116Agammaglobulinemia 3, autosomal recessiveEnrichmentCD79A2.28
117Immunodeficiency 92EnrichmentREL2.28
118Charcot-marie-tooth disease, demyelinating, type 1jEnrichmentITPR32.28
119Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.28
120Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.28
121Papillary tumor of the pineal regionEnrichmentPTEN2.28
122Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2EnrichmentAKT32.28
123Autoinflammation, antibody deficiency, and immune dysregulationEnrichmentPLCG22.28
124Long qt syndrome 16EnrichmentCALM32.28
125Immunodeficiency 14b, autosomal recessiveEnrichmentPIK3CD2.28
126Immunodeficiency, common variable, 3EnrichmentCD192.28
127Immunodeficiency 105, severe combinedEnrichmentPTPRC2.28
128Glioma susceptibility 2EnrichmentPTEN2.28
129Familial cold autoinflammatory syndrome 3EnrichmentPLCG22.28
130Takenouchi-kosaki syndromeEnrichmentCDC422.28
131Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.28
132Immunodeficiency 53EnrichmentRELB2.28
133Cd45 deficiencyEnrichmentPTPRC2.28
134Long qt syndrome 15EnrichmentCALM22.28
135Capillary hemangiomaEnrichmentAKT32.28
136Immunodeficiency 133 with ectodermal dysplasia with or without peripheral neuropathyEnrichmentITPR32.28
137Vegetative pyoderma gangrenosumEnrichmentPTPN62.28
138B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3)EnrichmentIGH2.28
139Bullous pyoderma gangrenosumEnrichmentPTPN62.28
140Agammaglobulinemia 3EnrichmentCD79A2.28
141Pustular pyoderma gangrenosumEnrichmentPTPN62.28
142Nocarh syndromeEnrichmentCDC422.28
143Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndromeEnrichmentPTEN2.28
144Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.28
145Classic pyoderma gangrenosumEnrichmentPTPN62.28
146Akt2-related familial partial lipodystrophyEnrichmentAKT22.28
147Endometrial cancerEnrichmentPIK3CA, PTEN2.27
148Hydrops fetalis, nonimmuneEnrichmentHRAS, PTPN112.22
149Colorectal cancerEnrichmentAKT1, PIK3CA, PIK3R12.15
150Non-immune hydrops fetalisEnrichmentHRAS, PTPN112.07
151Fibromatosis, gingival, 1EnrichmentSOS12.05
152Costello syndromeEnrichmentHRAS2.05
153Ovarian germ cell cancerEnrichmentCBL2.05
154Wiskott-aldrich syndromeEnrichmentWIPF12.05
155Immunodeficiency 33EnrichmentIKBKG2.05
156Pulmonic stenosisEnrichmentSOS12.05
157Isolated growth hormone deficiency, type iii, with agammaglobulinemiaEnrichmentBTK2.05
158Seizures, benign familial infantile, 2EnrichmentPRRT22.05
159Keratosis, seborrheicEnrichmentPIK3CA2.05
160Noonan syndrome 8EnrichmentPIK3CA2.05
161Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.05
162Myopia 28, autosomal recessiveEnrichmentDOK12.05
163Agammaglobulinemia, x-linkedEnrichmentBTK2.05
164Werner syndromeEnrichmentPTPN112.05
165Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.05
166Autoimmune disease, multisystem, infantile-onset, 3EnrichmentCBLB2.05
167Rela fusion-positive ependymomaEnrichmentRELA2.05
168Lymphoproliferative syndromeEnrichmentITK2.05
169Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.05
170Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.05
171Immunodeficiency 52EnrichmentLAT2.05
172Joint contractures, osteochondromas, and b-cell lymphomaEnrichmentNFATC22.05
173ArthritisEnrichmentSYK2.05
174Malignant germ cell tumor of ovaryEnrichmentCBL2.05
175Common variable immunodeficiency 12EnrichmentNFKB12.05
176Prrt2-related disorderEnrichmentPRRT22.05
177Tafro syndromeEnrichmentMAP2K22.05
178Wooly hair nevusEnrichmentHRAS2.05
179Prostate cancerEnrichmentPIK3CA, PTEN2.00
180Spinocerebellar ataxia 29EnrichmentITPR11.98
181Immunodeficiency, common variable, 2EnrichmentCR21.98
182Agammaglobulinemia 4, autosomal recessiveEnrichmentBLNK1.98
183Agammaglobulinemia 6, autosomal recessiveEnrichmentCD79B1.98
184Ventricular tachycardia, catecholaminergic polymorphic, 4EnrichmentCALM11.98
185Roifman-chitayat syndromeEnrichmentPIK3CD1.98
186Immunodeficiency, common variable, 10EnrichmentNFKB21.98
187Long qt syndrome 14EnrichmentCALM11.98
188Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC11.98
189Intravascular large b-cell lymphomaEnrichmentBCL61.98
190Immunodeficiency, common variable, 7EnrichmentCR21.98
191Senior-loken syndrome 7EnrichmentAKT31.98
192Agammaglobulinemia 4EnrichmentBLNK1.98
193Agammaglobulinemia 6EnrichmentCD79B1.98
194Immunodeficiency 104, severe combinedEnrichmentPTPRC1.98
195Bardet-biedl syndrome 16EnrichmentAKT31.98
196Vacterl with hydrocephalusEnrichmentPTEN1.98
197Primary mediastinal large b-cell lymphomaEnrichmentBCL61.98
198Juvenile polyposis of infancyEnrichmentPTEN1.98
199Ovarian cancerEnrichmentAKT1, MAP3K1, PIK3CA1.98
200Long qt syndromeEnrichmentCALM1, CALM21.94
201Ectodermal dysplasia and immunodeficiency 2EnrichmentNFKBIA1.91
202Pompe disease, infantile-onsetEnrichmentPIK3CA1.87
203Nuchal bleb, familialEnrichmentSOS11.87
204Langerhans cell histiocytosisEnrichmentMAP2K11.87
205Glut1 deficiency syndrome 2EnrichmentPRRT21.87
206Large congenital melanocytic nevusEnrichmentHRAS1.87
207Wieacker-wolff syndromeEnrichmentRASA11.87
208SpermatocytomaEnrichmentHRAS1.87
209Tricuspid valve insufficiencyEnrichmentPTPN111.87
210KeratoacanthomaEnrichmentPIK3CA1.87
211Gillespie syndromeEnrichmentITPR11.81
212Systemic lupus erythematosus 9EnrichmentCR21.81
213Neutrophilic dermatosis, acute febrileEnrichmentPTPN61.81
214High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL61.81
215Laryngeal squamous cell carcinomaEnrichmentPTEN1.81
216Systemic lupus erythematosusEnrichmentCR2, FCGR2B1.75
217Paroxysmal nonkinesigenic dyskinesia 1EnrichmentPRRT21.75
218Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS1.75
219Episodic kinesigenic dyskinesia 1EnrichmentPRRT21.75
220Neurofibromatosis-noonan syndromeEnrichmentMAP2K21.75
221Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK11.75
222Congenital generalized lipodystrophyEnrichmentFOS1.75
223Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalitiesEnrichmentGAD11.75
224Cerebrovascular diseaseEnrichmentPIK3CA1.75
225Spastic quadriplegic cerebral palsyEnrichmentGAD11.75
226Epidermolytic nevusEnrichmentHRAS1.75
227Familial cerebral cavernous malformationsEnrichmentPIK3CA1.75
228Familial paroxysmal nonkinesigenic dyskinesiaEnrichmentPRRT21.75
229Knobloch syndromeEnrichmentPAK21.75
230Familial or sporadic hemiplegic migraineEnrichmentPRRT21.75
231Gingival fibromatosisEnrichmentSOS11.75
232Nasopharyngeal carcinomaEnrichmentNFKBIA1.74
233Immunodeficiency, common variable, 1EnrichmentNFKB21.68
234Spinocerebellar ataxia 15EnrichmentITPR11.68
235Mantle cell lymphomaEnrichmentIGH1.68
236GliomaEnrichmentPTEN1.68
237Male infertility due to gonadal dysgenesis or sperm disorderEnrichmentSOS21.68
238Gastric cancerEnrichmentPIK3CA, PTEN1.67
239Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.65
240Convulsions, familial infantile, with paroxysmal choreoathetosisEnrichmentPRRT21.65
241Knobloch syndrome 1EnrichmentPAK21.65
242LymphomaEnrichmentPTPN111.65
243Myeloproliferative neoplasmEnrichmentCBL1.65
244Histiocytoid hemangiomaEnrichmentFOS1.65
245Self-limited infantile epilepsyEnrichmentPRRT21.65
246Aggressive systemic mastocytosisEnrichmentCBL1.65
247Lymphoma, mucosa-associated lymphoid typeEnrichmentIGH1.59
248Macrocephaly/autism syndromeEnrichmentPTEN1.59
249HemangiomaEnrichmentPTEN1.59
250Acute megakaryocytic leukemiaEnrichmentPTEN1.59
251Telangiectasia, hereditary hemorrhagic, type 1EnrichmentRASA11.57
252Hemihyperplasia, isolatedEnrichmentPIK3CA1.57
253Hemangioma, capillary infantileEnrichmentRASA11.57
254Basal cell carcinoma 1EnrichmentRASA11.57
255Patent ductus arteriosusEnrichmentPTPN111.57
256Lung squamous cell carcinomaEnrichmentPIK3CA1.57
257Ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathyEnrichmentCALM11.51
258Spinocerebellar ataxia, autosomal recessive 16EnrichmentITPR11.51
259Gallbladder cancerEnrichmentPIK3CA1.51
260Hereditary hemorrhagic telangiectasiaEnrichmentRASA11.51
261Pilomyxoid astrocytomaEnrichmentRAF11.51
262Overgrowth syndromeEnrichmentPIK3R11.51
263Squamous cell carcinoma, head and neckEnrichmentPTEN1.44
264MegacolonEnrichmentAKT31.44
265Coronary heart disease 5EnrichmentIKBKG1.40
266Adult hepatocellular carcinomaEnrichmentPIK3CA1.40
267Catecholaminergic polymorphic ventricular tachycardia 1EnrichmentCALM11.39
268Ciliary dyskinesia, primary, 3EnrichmentNFKB11.36
269Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.34
270Lennox-gastaut syndromeEnrichmentMAPK101.32
271Pectus excavatumEnrichmentPTPN111.32
272Immune deficiency diseaseEnrichmentSYK1.32
27346,xy complete gonadal dysgenesisEnrichmentMAP3K11.32
274PolymicrogyriaEnrichmentAKT31.29
275MelanomaEnrichmentPTEN1.29
276EpicanthusEnrichmentPTPN111.28
277Congenital long qt syndromeEnrichmentPTPN111.28
278Inflammatory bowel disease 1EnrichmentPRKCQ1.27
279Meningioma, familialEnrichmentPTEN1.25
280Uterine corpus cancerEnrichmentPTEN1.25
281Aortic valve disease 1EnrichmentSOS11.24
282Generalized epilepsy with febrile seizures plusEnrichmentPRRT21.21
283Lynch syndromeEnrichmentPIK3CA1.18
284Nk-cell enteropathyEnrichmentPIK3CB1.18
285Multiple sclerosisEnrichmentITPR11.15
286Anterior segment dysgenesisEnrichmentITPR11.12
287Heart, malformation ofEnrichmentMAPK11.11
288Patent foramen ovaleEnrichmentPTPN111.11
289Sudden infant death syndromeEnrichmentCALM21.07
290Autism spectrum disorderEnrichmentMAP2K1, PTPN111.06
291Cardiomyopathy, dilated, 1aEnrichmentNFATC21.04
292GliosarcomaEnrichmentNFKBIA1.03
293Hepatocellular carcinomaEnrichmentPIK3CA1.02
294Giant cell glioblastomaEnrichmentNFKBIA1.00
295Cardiomyopathy, familial hypertrophic, 1EnrichmentRAF10.99
296ScoliosisEnrichmentPTPN110.99
297MicrocephalyEnrichmentMAPK1, PTPN110.98
298StrabismusEnrichmentPTPN110.94
299Differentiated thyroid carcinomaEnrichmentHRAS0.91
300Lung cancerEnrichmentPIK3CA0.87
301Familial hypertrophic cardiomyopathyEnrichmentRAF10.86
302Severe combined immunodeficiencyEnrichmentIKBKB0.86
303Left ventricular noncompactionEnrichmentRAF10.84
304Hypertrophic cardiomyopathyEnrichmentPTPN110.75
305ThrombocytopeniaEnrichmentPTPN110.71
306Type 2 diabetes mellitusEnrichmentAKT20.70
307HypertelorismEnrichmentPIK3CA0.68
308Familial isolated dilated cardiomyopathyEnrichmentRAF10.67
309Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPTPN110.65
310Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA0.64
311Spastic ataxiaEnrichmentITPR10.61
312Hereditary breast ovarian cancer syndromeEnrichmentPTEN0.60
313Myeloma, multipleEnrichmentPIK3R20.59
314Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA0.59
315Dilated cardiomyopathyEnrichmentRAF10.52
316Congenital nervous system abnormalityEnrichmentPTEN0.37
317Nervous system diseaseEnrichmentPTEN0.37
318Inherited cancer-predisposing syndromeEnrichmentPTPN110.35

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