p38 MAPK signaling pathway (Pathway Interaction Database)

No Pathway Network information available for p38 MAPK signaling pathway (Pathway Interaction Database)

Pathways in the p38 MAPK signaling pathway (Pathway Interaction Database) SuperPath

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

Disorders associated with p38 MAPK signaling pathway (Pathway Interaction Database) SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.85
246,xy sex reversal 6EnrichmentMAP3K12.85
3Frontometaphyseal dysplasia 2EnrichmentMAP3K72.85
4Developmental delay with or without intellectual impairment or behavioral abnormalitiesEnrichmentTAOK12.85
5Intellectual developmental disorder, autosomal dominant 54EnrichmentCAMK2B2.85
6Endometrial serous adenocarcinomaEnrichmentATM2.85
7B-cell non-hodgkin lymphomaEnrichmentATM2.85
8Cerebral cavernous malformations 5EnrichmentMAP3K32.85
9Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.85
10Verrucous hemangiomaEnrichmentMAP3K32.85
11Polyvalvular heart disease syndromeEnrichmentTAB22.85
12Autosomal dominant non-syndromic intellectual disabilityEnrichmentCAMK2B, TAOK12.66
13MacroglossiaEnrichmentTAOK12.55
14Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.55
15Cardiac valvular dysplasia, x-linkedEnrichmentATM2.55
16Neurodevelopmental disorder with developmental delay and with or without motor or speech delayEnrichmentTAOK12.55
17Cerebral cavernous malformations 2EnrichmentCCM22.55
18High grade gliomaEnrichmentATM2.55
19Congenital heart defects, multiple types, 2EnrichmentTAB22.55
20T-cell prolymphocytic leukemiaEnrichmentATM2.55
21Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB22.55
22Cerebral cavernous malformationsEnrichmentCCM22.38
23Pelvic organ prolapseEnrichmentTAB22.38
24Ataxia-telangiectasiaEnrichmentATM2.38
25Polycythemia veraEnrichmentATM2.38
26Koolen-de vries syndromeEnrichmentATM2.38
27Frontometaphyseal dysplasiaEnrichmentMAP3K72.38
28AdenocarcinomaEnrichmentATM2.38
29Cavernous hemangiomaEnrichmentCCM22.38
30Diffuse gastric and lobular breast cancer syndromeEnrichmentMAP3K62.25
31Mantle cell lymphomaEnrichmentATM2.25
32Familial cerebral cavernous malformationsEnrichmentCCM22.25
33Oculomotor apraxiaEnrichmentATM2.25
34Ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominantEnrichmentTRAF62.16
35GlioblastomaEnrichmentATM2.16
36Clear cell renal cell carcinomaEnrichmentATM2.08
37Ovarian cancerEnrichmentATM, MAP3K12.06
38Renal cell carcinoma, papillary, 1EnrichmentATM2.01
39Fanconi anemia, complementation group cEnrichmentTAOK11.95
40Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.90
41Colonic benign neoplasmEnrichmentATM1.90
42Lynch syndrome 1EnrichmentATM1.86
43Leukemia, chronic lymphocyticEnrichmentATM1.86
44Migraine with or without aura 1EnrichmentTAB21.82
45Immune deficiency diseaseEnrichmentATM1.82
4646,xy complete gonadal dysgenesisEnrichmentMAP3K11.82
47Uterine corpus cancerEnrichmentATM1.82
48Familial colorectal cancer type xEnrichmentATM1.82
49Aortic valve disease 1EnrichmentTAB21.74
50Breast-ovarian cancer, familial 1EnrichmentATM1.74
5146,xy partial gonadal dysgenesisEnrichmentMAP3K11.71
52Renal cell carcinoma, nonpapillaryEnrichmentATM1.68
53GliosarcomaEnrichmentATM1.65
54Giant cell glioblastomaEnrichmentATM1.63
55Patent foramen ovaleEnrichmentTAB21.60
56Endometrial cancerEnrichmentATM1.54
57Pancreatic cancerEnrichmentATM1.46
58Bladder cancerEnrichmentATM1.40
59Prostate cancerEnrichmentATM1.40
60DystoniaEnrichmentCAMK2B1.32
61Gastric cancerEnrichmentATM1.23
62Hereditary breast carcinomaEnrichmentATM1.22
63Hereditary breast ovarian cancer syndromeEnrichmentATM1.13
64Myeloma, multipleEnrichmentATM1.12
65Breast cancerEnrichmentATM1.00
66Dilated cardiomyopathyEnrichmentTAB20.97
67Colorectal cancerEnrichmentATM0.94
68Congenital nervous system abnormalityEnrichmentCAMK2B0.86
69Nervous system diseaseEnrichmentCAMK2B0.86
70MicrocephalyEnrichmentCAMK2B0.80
71Inherited cancer-predisposing syndromeEnrichmentATM0.77

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