Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways

No Pathway Network information available for Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways

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

Disorders associated with Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Autoinflammatory diseaseEnrichmentMEFV, NLRC4, NLRP3, NOD25.58
2Behcet syndromeEnrichmentMEFV, NOD2, PSTPIP14.21
3Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.46
4Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.58
5Immunodeficiency 103 fungal infectionsEnrichmentCARD92.58
6Incontinentia pigmentiEnrichmentIKBKG2.58
7Autoinflammatory disease, systemic, x-linkedEnrichmentIKBKG2.58
8Caspase 8 deficiencyEnrichmentCASP82.58
9Fetal encasement syndromeEnrichmentCHUK2.58
10Blau syndromeEnrichmentNOD22.58
11Frontometaphyseal dysplasia 2EnrichmentMAP3K72.58
12Immunodeficiency 15bEnrichmentIKBKB2.58
13Immunodeficiency 15aEnrichmentIKBKB2.58
14Ectodermal dysplasia and immunodeficiency 1EnrichmentIKBKG2.58
15Autoimmune disease, multisystem, with facial dysmorphismEnrichmentITCH2.58
16Bartsocas-papas syndrome 2EnrichmentCHUK2.58
17Intellectual developmental disorder, autosomal recessive 80, with variant lissencephalyEnrichmentCASP22.58
18Familial behcet-like autoinflammatory syndromeEnrichmentTNFAIP32.58
19Syndromic multisystem autoimmune disease due to itch deficiencyEnrichmentITCH2.58
20Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to ikbka deficiencyEnrichmentCHUK2.58
21Polyvalvular heart disease syndromeEnrichmentTAB22.58
22Cinca syndromeEnrichmentNLRP32.38
23Keratoendotheliitis fugax hereditariaEnrichmentNLRP32.38
24Pyogenic sterile arthritis, pyoderma gangrenosum, and acneEnrichmentPSTPIP12.38
25Vitiligo-associated multiple autoimmune disease susceptibility 1EnrichmentNLRP12.38
26Familial cold autoinflammatory syndrome 1EnrichmentNLRP32.38
27Muckle-wells syndromeEnrichmentNLRP32.38
28Autoinflammatory syndrome with cytopenia, hyperzincemia, and hypercalprotectinemiaEnrichmentPSTPIP12.38
29Deafness, autosomal dominant 34, with or without inflammationEnrichmentNLRP32.38
30Respiratory papillomatosis, juvenile recurrent, congenitalEnrichmentNLRP12.38
31Familial cold autoinflammatory syndrome 4EnrichmentNLRC42.38
32Autoinflammation with infantile enterocolitisEnrichmentNLRC42.38
33Cerebral amyloid angiopathy, app-relatedEnrichmentAPP2.38
34Palmoplantar carcinoma, multiple self-healingEnrichmentNLRP12.38
35Heme oxygenase 1 deficiencyEnrichmentHMOX12.38
36Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.38
37Autoinflammation with arthritis and dyskeratosisEnrichmentNLRP12.38
38Cryopyrin associated periodic syndromeEnrichmentNLRP32.38
39Familial amyloid nephropathy with urticaria and deafnessEnrichmentNLRP32.38
40Periodic fever-infantile enterocolitis-autoinflammatory syndromeEnrichmentNLRC42.38
41Systemic lupus erythematosusEnrichmentIRAK1, TNFAIP32.32
42Cylindromatosis, familialEnrichmentCYLD2.28
43Trichoepithelioma, multiple familial, 1EnrichmentCYLD2.28
44Immunodeficiency 33EnrichmentIKBKG2.28
45Yao syndromeEnrichmentNOD22.28
46Autoinflammatory syndrome, familial, behcet-like 1EnrichmentTNFAIP32.28
47Frontotemporal dementia and/or amyotrophic lateral sclerosis 8EnrichmentCYLD2.28
48Brooke-spiegler syndromeEnrichmentCYLD2.28
49Ectodermal dysplasia and immune deficiencyEnrichmentIKBKG2.28
50Congenital heart defects, multiple types, 2EnrichmentTAB22.28
51Glucosephosphate dehydrogenase deficiencyEnrichmentIKBKG2.28
52Crohn's diseaseEnrichmentNOD22.28
53Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB22.28
54Submucosal cleft palateEnrichmentUBB2.28
55Cleft hard palateEnrichmentUBB2.28
56Pelvic organ prolapseEnrichmentTAB22.10
57Uvula, bifidEnrichmentUBB2.10
58Cleft soft palateEnrichmentUBB2.10
59Frontometaphyseal dysplasiaEnrichmentMAP3K72.10
60Cerebral amyloid angiopathy, cst3-relatedEnrichmentAPP2.08
61Familial mediterranean fever, autosomal dominantEnrichmentMEFV2.08
62Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.08
63Immunodeficiency, common variable, 10EnrichmentNFKB22.08
64Familial mediterranean feverEnrichmentMEFV2.08
65Oocyte/zygote/embryo maturation arrest 7EnrichmentPANX12.08
66Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.08
67Intravascular large b-cell lymphomaEnrichmentBCL22.08
68Rela fusion-positive ependymomaEnrichmentRELA2.08
69Pericardial effusionEnrichmentNLRP32.08
70Intermittent hydrarthrosisEnrichmentMEFV2.08
71Common variable immunodeficiency 12EnrichmentNFKB12.08
72Pediatric systemic lupus erythematosusEnrichmentIRAK11.98
73Neutrophilic dermatosis, acute febrileEnrichmentMEFV1.91
74High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL21.91
75Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF61.88
76Lymphoma, mucosa-associated lymphoid typeEnrichmentBIRC31.88
77Anemia, congenital, nonspherocytic hemolytic, 1EnrichmentIKBKG1.88
78Immunodeficiency, common variable, 1EnrichmentNFKB21.78
79Follicular lymphomaEnrichmentBCL21.69
80Female infertility due to oocyte meiotic arrestEnrichmentPANX11.69
81Inflammatory bowel disease 1EnrichmentNOD21.63
82Coronary heart disease 5EnrichmentIKBKG1.63
83Adult hepatocellular carcinomaEnrichmentCASP81.63
84Alzheimer's disease 1EnrichmentAPP1.54
85Early-onset autosomal dominant alzheimer diseaseEnrichmentAPP1.54
86Migraine with or without aura 1EnrichmentTAB21.54
87Aortic valve disease 1EnrichmentTAB21.47
88Leukemia, chronic lymphocyticEnrichmentP2RX71.39
89Ciliary dyskinesia, primary, 3EnrichmentNFKB11.39
90Patent foramen ovaleEnrichmentTAB21.33
91Pulmonary disease, chronic obstructiveEnrichmentHMOX11.28
92Alzheimer's diseaseEnrichmentAPP1.28
93Hepatocellular carcinomaEnrichmentCASP81.25
94MalariaEnrichmentIKBKG1.23
95Neuronal ceroid lipofuscinosisEnrichmentMEFV1.22
96Kidney diseaseEnrichmentMEFV1.22
97Alzheimer disease, familial, 1EnrichmentAPP1.17
98Arteriovenous malformations of the brainEnrichmentNLRP31.12
99Lung cancerEnrichmentCASP81.09
100Severe combined immunodeficiencyEnrichmentIKBKB1.08
101Cystic fibrosisEnrichmentHMOX10.91
102Myeloma, multipleEnrichmentCYLD0.86
103Breast cancerEnrichmentCASP80.74
104Dilated cardiomyopathyEnrichmentTAB20.72
105Inherited cancer-predisposing syndromeEnrichmentCYLD0.53

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