Regulated Necrosis

Pathway network for the Regulated Necrosis SuperPath

Sources:
  • Reactome

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

Disorders associated with Regulated Necrosis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Gastric cancerEnrichmentIL1B, IRF1, TP534.36
2Lung cancerEnrichmentCASP8, IRF1, PRKN3.95
3Adult hepatocellular carcinomaEnrichmentCASP8, TP533.52
4Lung cancer susceptibility 3EnrichmentPRKN, TP533.12
5Caspase 8 deficiencyEnrichmentCASP82.88
6Leprosy 2EnrichmentPRKN2.88
7Autoimmune disease, multisystem, with facial dysmorphismEnrichmentITCH2.88
8Immunodeficiency 90 with encephalopathy, functional hyposplenia, and hepatic dysfunctionEnrichmentFADD2.88
9Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.88
10Syndromic multisystem autoimmune disease due to itch deficiencyEnrichmentITCH2.88
11Brachyphalangy, polydactyly, and tibial aplasia/hypoplasiaEnrichmentHMGB12.79
12Cataract 31, multiple typesEnrichmentCHMP4B2.79
13Bone marrow failure syndrome 5EnrichmentTP532.79
14Papilloma of choroid plexusEnrichmentTP532.79
15Basal cell carcinoma 7EnrichmentTP532.79
16Anaplastic thyroid carcinomaEnrichmentTP532.79
17Deafness, autosomal dominant 5EnrichmentGSDME2.79
18Ductal carcinoma in situEnrichmentTP532.79
19Thyroid gland undifferentiated carcinomaEnrichmentTP532.79
20Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.79
21Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.79
22Choroid plexus cancerEnrichmentTP532.79
23Pleomorphic xanthoastrocytomaEnrichmentTP532.79
24Hepatocellular carcinomaEnrichmentCASP8, TP532.72
25Parkinson disease 12EnrichmentPRKN2.58
26Spinocerebellar ataxia 48EnrichmentSTUB12.58
27Immunodeficiency 57 with autoinflammationEnrichmentRIPK12.58
28Oculootodental syndromeEnrichmentFADD2.58
29Submucosal cleft palateEnrichmentUBB2.58
30Cleft hard palateEnrichmentUBB2.58
31Cyclic neutropeniaEnrichmentELANE2.49
32Adrenocortical carcinoma, hereditaryEnrichmentTP532.49
33Neutropenia, severe congenital, x-linkedEnrichmentELANE2.49
34Cervical cancerEnrichmentTP532.49
35Lymphoma, hodgkin, classicEnrichmentTP532.49
36Congenital fibrosarcomaEnrichmentTP532.49
37Li-fraumeni syndrome 1EnrichmentTP532.49
38SarcomaEnrichmentTP532.49
39Cervix carcinomaEnrichmentTP532.49
40Hodgkin's lymphomaEnrichmentTP532.49
41Immunodeficiency 117EnrichmentIRF12.49
42Pleomorphic rhabdomyosarcomaEnrichmentTP532.49
43Uvula, bifidEnrichmentUBB2.40
44Cleft soft palateEnrichmentUBB2.40
45Neutropenia, severe congenital, 1, autosomal dominantEnrichmentELANE2.31
46Osteogenic sarcomaEnrichmentTP532.31
47Nasopharyngeal carcinomaEnrichmentTP532.31
48Atypical teratoid rhabdoid tumorEnrichmentTP532.31
49Anaplastic astrocytomaEnrichmentTP532.31
50Squamous cell carcinomaEnrichmentTP532.31
51AdenocarcinomaEnrichmentTP532.31
52Bone osteosarcomaEnrichmentTP532.31
53Complex hereditary spastic paraplegiaEnrichmentPRKN2.28
54Small cell cancer of the lungEnrichmentTP532.19
55Thyroid cancer, nonmedullary, 1EnrichmentTP532.19
56Lung sarcomatoid carcinomaEnrichmentTP532.19
57Embryonal rhabdomyosarcomaEnrichmentTP532.19
58Lymphoma, mucosa-associated lymphoid typeEnrichmentBIRC32.18
59Parkinson disease 2, autosomal recessive juvenileEnrichmentPRKN2.18
60Parkin type of early-onset parkinson diseaseEnrichmentPRKN2.18
61Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK12.10
62Spinocerebellar ataxia, autosomal recessive 16EnrichmentSTUB12.10
63Il10-related early-onset inflammatory bowel diseaseEnrichmentRIPK12.10
64Cataract 6, multiple typesEnrichmentCHMP4B2.09
65Rhabdomyosarcoma 2EnrichmentTP532.09
66LymphomaEnrichmentTP532.09
67Acute megakaryocytic leukemiaEnrichmentTP532.09
68Autosomal dominant severe congenital neutropeniaEnrichmentELANE2.09
69Li-fraumeni syndromeEnrichmentTP532.01
70Adrenocortical carcinomaEnrichmentTP532.01
71Breast adenocarcinomaEnrichmentTP532.01
72Esophageal cancerEnrichmentTP531.95
73Squamous cell carcinoma, head and neckEnrichmentTP531.95
74Semantic dementiaEnrichmentCHMP2B1.95
75NeutropeniaEnrichmentELANE1.95
76Essential thrombocythemiaEnrichmentTP531.95
77Gallbladder cancerEnrichmentTP531.95
78B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentTP531.95
79Hereditary breast ovarian cancer syndromeEnrichmentRIPK1, TP531.94
80Glioma susceptibility 1EnrichmentTP531.89
81Lymphoma, non-hodgkin, familialEnrichmentTP531.89
82Early-onset posterior polar cataractEnrichmentCHMP4B1.89
83Immune deficiency diseaseEnrichmentRIPK11.84
84Progressive non-fluent aphasiaEnrichmentCHMP2B1.84
85Primary hyperaldosteronismEnrichmentTP531.84
86Behavioral variant of frontotemporal dementiaEnrichmentCHMP2B1.84
87Early-onset parkinson's diseaseEnrichmentPRKN1.80
88Leukemia, chronic lymphocyticEnrichmentTP531.79
89Familial colorectal cancerEnrichmentTP531.79
90Myelodysplastic syndromeEnrichmentTP531.75
91Lung non-small cell carcinomaEnrichmentIRF11.75
92Lip and oral cavity carcinomaEnrichmentTP531.71
93Breast cancerEnrichmentCASP8, TP531.69
94Parkinson's diseaseEnrichmentPRKN1.60
95RhabdomyosarcomaEnrichmentTP531.59
96GliosarcomaEnrichmentTP531.59
97Giant cell glioblastomaEnrichmentTP531.56
98Diffuse large b-cell lymphomaEnrichmentTP531.52
99Parkinson disease, late-onsetEnrichmentPRKN1.50
100HepatoblastomaEnrichmentTP531.47
101Ovarian cancerEnrichmentPRKN, TP531.45
102Diamond-blackfan anemia 1EnrichmentTP531.44
103Autoinflammatory diseaseEnrichmentELANE1.42
104Pancreatic cancerEnrichmentTP531.40
105Bladder cancerEnrichmentTP531.34
106Prostate cancerEnrichmentTP531.34
107Systemic lupus erythematosusEnrichmentUBE2L31.30
108Diamond-blackfan anemiaEnrichmentTP531.25
109Leukemia, acute myeloidEnrichmentTP531.20
110Hereditary breast carcinomaEnrichmentTP531.16
111SchizophreniaEnrichmentPRKN1.12
112Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentGSDME1.09
113Myeloma, multipleEnrichmentTP531.06
114Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentCHMP2B1.05
115AutismEnrichmentPRKN1.04
116Rare genetic deafnessEnrichmentGSDME0.92
117Colorectal cancerEnrichmentTP530.88
118Autism spectrum disorderEnrichmentPRKN0.87
119Inherited cancer-predisposing syndromeEnrichmentTP530.71

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