Validated nuclear estrogen receptor alpha network

No Pathway Network information available for Validated nuclear estrogen receptor alpha network

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

Disorders associated with Validated nuclear estrogen receptor alpha network SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Colorectal cancerEnrichmentAXIN2, BRCA1, CCND1, EP300, SMAD44.23
2Myeloma, multipleEnrichmentCCND1, HDAC4, NCOR22.61
3Palmoplantar keratoderma, punctate type iiEnrichmentBRCA12.32
4Keratitis-ichthyosis-deafness syndrome, autosomal recessiveEnrichmentAP1B12.32
5Oligodontia-colorectal cancer syndromeEnrichmentAXIN22.32
6Hemolytic uremic syndrome, atypical 5EnrichmentC32.32
7Fetal encasement syndromeEnrichmentCHUK2.32
8Ceroid lipofuscinosis, neuronal, 10EnrichmentCTSD2.32
946,xy sex reversal 2EnrichmentNR0B12.32
10Adrenal hypoplasia, congenitalEnrichmentNR0B12.32
11Chromosome 2q37 deletion syndromeEnrichmentHDAC42.32
12Progesterone resistanceEnrichmentPGR2.32
13Infant-type hemispheric gliomaEnrichmentBRCA12.32
14Major affective disorder 7EnrichmentXBP12.32
15Ovarian dysgenesis 8EnrichmentESR22.32
16Ataxia-telangiectasia-like disorder 2EnrichmentPCNA2.32
17Macular degeneration, age-related, 9EnrichmentC32.32
18Complement component 3 deficiency, autosomal recessiveEnrichmentC32.32
19Congenital anomalies of kidney and urinary tract 3EnrichmentNRIP12.32
20Bartsocas-papas syndrome 2EnrichmentCHUK2.32
21Neurodevelopmental disorder with central hypotonia and dysmorphic faciesEnrichmentHDAC42.32
22Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomaliesEnrichmentABCA32.32
23Complement component 3 deficiencyEnrichmentC32.32
24Heritable thoracic aortic diseaseEnrichmentSMAD42.32
25Membranoproliferative glomerulonephritisEnrichmentC32.32
26Primary membranoproliferative glomerulonephritisEnrichmentC32.32
27Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.32
28Primary peritoneal carcinomaEnrichmentBRCA12.32
29Precursor t-cell acute lymphoblastic leukemiaEnrichmentMYC, SET2.27
30Breast cancerEnrichmentBRCA1, ESR1, JUN2.26
31Pancreatic cancerEnrichmentBRCA1, SMAD42.20
32Hirschsprung disease 1EnrichmentAXIN2, DSCAM2.07
33Burkitt lymphomaEnrichmentMYC2.02
34Myhre syndromeEnrichmentSMAD42.02
35Carbamoyl phosphate synthetase i deficiency, hyperammonemia due toEnrichmentABCA32.02
36Surfactant metabolism dysfunction, pulmonary, 1EnrichmentABCA32.02
37Juvenile polyposis/hereditary hemorrhagic telangiectasia syndromeEnrichmentSMAD42.02
38Ataxia, intention tremor, and hypotonia syndrome, childhood-onsetEnrichmentPOU4F12.02
39Fanconi anemia, complementation group sEnrichmentBRCA12.02
40Menke-hennekam syndrome 2EnrichmentEP3002.02
41Pancreatic cancer 4EnrichmentBRCA12.02
42Surfactant metabolism dysfunction, pulmonary, 3EnrichmentABCA32.02
43Glaucoma, primary closed-angleEnrichmentCOL18A12.02
44Spastic tetraplegia and axial hypotonia, progressiveEnrichmentSOD12.02
45Inflammatory breast carcinomaEnrichmentBRCA12.02
46Intellectual developmental disorder, autosomal dominant 58EnrichmentSET2.02
47Peritoneum cancerEnrichmentBRCA12.02
48Bilateral breast cancerEnrichmentBRCA12.02
49Thyroid carcinoma, familial medullaryEnrichmentESR21.84
50Juvenile polyposis syndromeEnrichmentSMAD41.84
51Niemann-pick disease, type aEnrichmentAPBB11.84
52Niemann-pick disease, type bEnrichmentAPBB11.84
53Mednik syndromeEnrichmentAP1B11.84
54Estrogen resistanceEnrichmentESR11.84
55Cerebellar dysfunction with variable cognitive and behavioral abnormalitiesEnrichmentPOU4F11.84
56High-grade b-cell lymphoma double-hit/triple-hitEnrichmentMYC1.84
57Migraine without auraEnrichmentESR11.84
58Genetic atypical hemolytic-uremic syndromeEnrichmentC31.84
59Pediatric acute respiratory distress syndromeEnrichmentABCA31.84
60Gastric cancerEnrichmentBRCA1, SMAD41.74
61Hereditary breast carcinomaEnrichmentBRCA1, ESR11.73
62Polyposis syndrome, hereditary mixed, 1EnrichmentBRCA11.72
63CholangiocarcinomaEnrichmentBRCA11.72
64Mantle cell lymphomaEnrichmentCCND11.72
65Arthrogryposis multiplex congenita 3, myogenic typeEnrichmentESR11.72
66Knobloch syndromeEnrichmentCOL18A11.72
67Niemann-pick disease, type c1EnrichmentAPBB11.62
68Von hippel-lindau syndromeEnrichmentCCND11.62
69Knobloch syndrome 1EnrichmentCOL18A11.62
70Amyotrophic lateral sclerosis 10 with or without frontotemporal dementiaEnrichmentSOD11.62
71Breast-ovarian cancer, familial 2EnrichmentBRCA11.62
72Rubinstein-taybi syndrome 2EnrichmentEP3001.62
73Pervasive developmental disorderEnrichmentPRDM151.62
74Niemann-pick diseaseEnrichmentAPBB11.62
75Nonsyndromic 46,xx testicular disorders/differences of sex developmentEnrichmentNR0B11.62
76Hereditary pulmonary alveolar proteinosisEnrichmentABCA31.62
77Generalized juvenile polyposis/juvenile polyposis coliEnrichmentSMAD41.62
78Rare pervasive developmental disorderEnrichmentPRDM151.62
79Inherited cancer-predisposing syndromeEnrichmentAXIN2, BRCA1, SMAD41.60
80Rubinstein-taybi syndrome 1EnrichmentEP3001.55
81Chromosome 16p13.3 deletion syndrome, proximalEnrichmentEP3001.55
82Renal hypoplasiaEnrichmentDDX541.55
83Atypical hemolytic uremic syndrome with complement gene abnormalityEnrichmentC31.55
84Motor neuron diseaseEnrichmentSOD11.48
85Gallbladder cancerEnrichmentSMAD41.48
86Hereditary hemorrhagic telangiectasiaEnrichmentSMAD41.48
87Tooth agenesis, selective, 1EnrichmentAXIN21.37
88Charge syndromeEnrichmentEP3001.37
89Loeys-dietz syndromeEnrichmentABCA31.37
90Amyotrophic lateral sclerosis 1EnrichmentSOD11.33
91Leukemia, chronic lymphocyticEnrichmentCCND11.33
92Migraine with or without aura 1EnrichmentESR11.29
9346,xy complete gonadal dysgenesisEnrichmentNR0B11.29
94Uterine corpus cancerEnrichmentBRCA11.29
95Breast-ovarian cancer, familial 1EnrichmentBRCA11.22
96Periventricular nodular heterotopiaEnrichmentBRCA11.19
97CataractEnrichmentCOL18A11.19
9846,xy partial gonadal dysgenesisEnrichmentNR0B11.19
99Polydactyly, postaxial, type a1EnrichmentEP3001.16
100Atypical hemolytic-uremic syndromeEnrichmentC31.16
101Neuronal ceroid lipofuscinosisEnrichmentCTSD1.16
102Rare genetic intellectual disabilityEnrichmentEP3001.16
103RhabdomyosarcomaEnrichmentBRCA11.13
104Interstitial lung disease 2EnrichmentABCA31.11
105Ovarian cancerEnrichmentAXIN2, BRCA11.07
106Endometrial cancerEnrichmentBRCA11.02
107Myocardial infarctionEnrichmentESR11.00
108Tooth agenesisEnrichmentAXIN21.00
109Bladder cancerEnrichmentBRCA10.89
110Prostate cancerEnrichmentBRCA10.89
111Stargardt disease 1EnrichmentCOL18A10.87
112Lung cancerEnrichmentBRCA10.85
113CakutEnrichmentNRIP10.82
114Fanconi anemia, complementation group aEnrichmentBRCA10.81
115Familial thoracic aortic aneurysm and aortic dissectionEnrichmentSMAD40.72
116ThrombocytopeniaEnrichmentSMAD40.69
117Body mass index quantitative trait locus 11EnrichmentNR0B20.67
118Autosomal dominant non-syndromic intellectual disabilityEnrichmentSET0.67
119Hereditary breast ovarian cancer syndromeEnrichmentBRCA10.63
120Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentSOD10.61
121MicrocephalyEnrichmentEP3000.35
122Retinitis pigmentosaEnrichmentCOL18A10.19
123Hereditary retinal dystrophyEnrichmentCOL18A10.12
124Fundus dystrophyEnrichmentCOL18A10.12

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