Apoptosis modulation and signaling

No Pathway Network information available for Apoptosis modulation and signaling

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

Disorders associated with Apoptosis modulation and signaling SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Squamous cell carcinoma, head and neckEnrichmentTNFRSF10B, TP533.95
2Lymphoproliferative syndrome, x-linked, 2EnrichmentXIAP2.63
3Parkinson disease 13, autosomal dominantEnrichmentHTRA22.63
4Bone marrow failure syndrome 5EnrichmentTP532.63
5Papilloma of choroid plexusEnrichmentTP532.63
6Basal cell carcinoma 7EnrichmentTP532.63
7Spermatogenic failure 99EnrichmentSEPTIN42.63
8Anaplastic thyroid carcinomaEnrichmentTP532.63
9Deeah syndromeEnrichmentMADD2.63
10Thrombocytopenia 4EnrichmentCYCS2.63
11Ductal carcinoma in situEnrichmentTP532.63
12Congenital heart defects and ectodermal dysplasiaEnrichmentPRKD12.63
13Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.63
14Neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotoniaEnrichmentMADD2.63
15Thyroid gland undifferentiated carcinomaEnrichmentTP532.63
16Small-cell carcinoma of the ovary of hypercalcemic typeEnrichmentTP532.63
17Intellectual developmental disorder, autosomal recessive 80, with variant lissencephalyEnrichmentCASP22.63
18Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtypeEnrichmentTP532.63
19Choroid plexus cancerEnrichmentTP532.63
20Pleomorphic xanthoastrocytomaEnrichmentTP532.63
21Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephalyEnrichmentPIDD12.63
22Malignant epithelial tumor of salivary glandsEnrichmentPRKD12.63
23Adrenocortical carcinoma, hereditaryEnrichmentTP532.33
24Spondyloepimetaphyseal dysplasia, x-linked, with hypomyelinating leukodystrophyEnrichmentAIFM12.33
25Charcot-marie-tooth disease, x-linked recessive, 4, with or without cerebellar ataxiaEnrichmentAIFM12.33
26Combined oxidative phosphorylation deficiency 6EnrichmentAIFM12.33
27Cervical cancerEnrichmentTP532.33
28Lymphoma, hodgkin, classicEnrichmentTP532.33
29Deafness, autosomal dominant 64EnrichmentDIABLO2.33
30Congenital fibrosarcomaEnrichmentTP532.33
31Li-fraumeni syndrome 1EnrichmentTP532.33
32SarcomaEnrichmentTP532.33
33Cervix carcinomaEnrichmentTP532.33
34Hodgkin's lymphomaEnrichmentTP532.33
35Immunodeficiency 57 with autoinflammationEnrichmentRIPK12.33
36Charcot-marie-tooth disease x-linked recessive 4EnrichmentAIFM12.33
37Pleomorphic rhabdomyosarcomaEnrichmentTP532.33
38Spinal muscular atrophy, type iiiEnrichmentNAIP2.15
39Spinal muscular atrophy, type iEnrichmentNAIP2.15
40Spinal muscular atrophy, type iiEnrichmentNAIP2.15
41Osteogenic sarcomaEnrichmentTP532.15
42Nasopharyngeal carcinomaEnrichmentTP532.15
43Deafness, x-linked 5, with peripheral neuropathyEnrichmentAIFM12.15
44X-linked deafness 5EnrichmentAIFM12.15
45Atypical teratoid rhabdoid tumorEnrichmentTP532.15
46Anaplastic astrocytomaEnrichmentTP532.15
47Squamous cell carcinomaEnrichmentTP532.15
48AdenocarcinomaEnrichmentTP532.15
49Combined oxidative phosphorylation deficiencyEnrichmentAIFM12.15
50Laryngeal squamous cell carcinomaEnrichmentTNFRSF10B2.15
51Bone osteosarcomaEnrichmentTP532.15
52Hereditary breast ovarian cancer syndromeEnrichmentRIPK1, TP532.13
53Small cell cancer of the lungEnrichmentTP532.03
54Thyroid cancer, nonmedullary, 1EnrichmentTP532.03
55Lymphoproliferative syndrome 2EnrichmentXIAP2.03
56Lung sarcomatoid carcinomaEnrichmentTP532.03
57Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1EnrichmentPTRH22.03
58Embryonal rhabdomyosarcomaEnrichmentTP532.03
593-methylglutaconic aciduria, type viiiEnrichmentHTRA22.03
60Rhabdomyosarcoma 2EnrichmentTP531.93
61LymphomaEnrichmentTP531.93
62Acute megakaryocytic leukemiaEnrichmentTP531.93
63Autosomal thrombocytopenia with normal plateletsEnrichmentCYCS1.93
64Multiple acyl-coa dehydrogenase deficiency, severe neonatal typeEnrichmentMADD1.93
65Li-fraumeni syndromeEnrichmentTP531.85
66Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK11.85
67Adrenocortical carcinomaEnrichmentTP531.85
68Il10-related early-onset inflammatory bowel diseaseEnrichmentRIPK11.85
69Breast adenocarcinomaEnrichmentTP531.85
70Esophageal cancerEnrichmentTP531.79
71Essential thrombocythemiaEnrichmentTP531.79
72Gallbladder cancerEnrichmentTP531.79
73B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)EnrichmentTP531.79
74Glioma susceptibility 1EnrichmentTP531.73
75Lymphoma, non-hodgkin, familialEnrichmentTP531.73
76Male infertility due to globozoospermiaEnrichmentSEPTIN41.73
77Adult hepatocellular carcinomaEnrichmentTP531.68
78Primary hyperaldosteronismEnrichmentTP531.68
79Leukemia, chronic lymphocyticEnrichmentTP531.63
80Familial colorectal cancerEnrichmentTP531.63
81Immune deficiency diseaseEnrichmentRIPK11.59
82Myelodysplastic syndromeEnrichmentTP531.59
83Early-onset parkinson's diseaseEnrichmentHTRA21.55
84Lip and oral cavity carcinomaEnrichmentTP531.55
85Lung cancer susceptibility 3EnrichmentTP531.49
86RhabdomyosarcomaEnrichmentTP531.43
87GliosarcomaEnrichmentTP531.43
88Giant cell glioblastomaEnrichmentTP531.40
89Diffuse large b-cell lymphomaEnrichmentTP531.36
90LeukodystrophyEnrichmentAIFM11.34
91HepatoblastomaEnrichmentTP531.31
92Hepatocellular carcinomaEnrichmentTP531.30
93Diamond-blackfan anemia 1EnrichmentTP531.28
94Ear malformationEnrichmentAIFM11.26
95Autoinflammatory diseaseEnrichmentXIAP1.26
96Pancreatic cancerEnrichmentTP531.24
97Auditory neuropathyEnrichmentAIFM11.22
98Bladder cancerEnrichmentTP531.18
99Prostate cancerEnrichmentTP531.18
100Diamond-blackfan anemiaEnrichmentTP531.09
101Leukemia, acute myeloidEnrichmentTP531.04
102Gastric cancerEnrichmentTP531.01
103Hereditary breast carcinomaEnrichmentTP531.01
104Sensorineural hearing lossEnrichmentAIFM10.97
105ThrombocytopeniaEnrichmentCYCS0.97
106Rare autosomal dominant non-syndromic sensorineural deafness type dfnaEnrichmentDIABLO0.94
107Myeloma, multipleEnrichmentTP530.91
108Breast cancerEnrichmentTP530.79
109Colorectal cancerEnrichmentTP530.73
110Ovarian cancerEnrichmentTP530.67
111Complex neurodevelopmental disorderEnrichmentMADD0.59
112Inherited cancer-predisposing syndromeEnrichmentTP530.57

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