p38 MAPK signaling pathway (WikiPathways)

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

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

Disorders associated with p38 MAPK signaling pathway (WikiPathways) SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Loeys-dietz syndromeEnrichmentTGFB2, TGFBR13.66
2Marfan syndromeEnrichmentTGFB2, TGFBR13.57
3Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.60
4Multiple self-healing squamous epitheliomaEnrichmentTGFBR12.60
546,xy sex reversal 6EnrichmentMAP3K12.60
6Frontometaphyseal dysplasia 2EnrichmentMAP3K72.60
7Camurati-engelmann disease 2EnrichmentTGFB22.60
8Charcot-marie-tooth disease, axonal, type 2fEnrichmentHSPB12.60
9Immunodeficiency 31aEnrichmentSTAT12.60
10Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorderEnrichmentPLA2G4A2.60
11Polydactyly-macrocephaly syndromeEnrichmentMAX2.60
12Immunodeficiency 31bEnrichmentSTAT12.60
13Neurocardiofaciodigital syndromeEnrichmentMAPKAPK52.60
14Gastrointestinal ulceration, recurrent, with dysfunctional plateletsEnrichmentPLA2G4A2.60
15Takenouchi-kosaki syndromeEnrichmentCDC422.60
16Autoinflammation with episodic fever and lymphadenopathyEnrichmentRIPK12.60
17Nocarh syndromeEnrichmentCDC422.60
18Cryptogenic multifocal ulcerous stenosing enteritisEnrichmentPLA2G4A2.60
19Phakomatosis pigmentokeratoticaEnrichmentHRAS2.60
20Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndromEnrichmentRAC12.60
21Burkitt lymphomaEnrichmentMYC2.30
22Costello syndromeEnrichmentHRAS2.30
23Loeys-dietz syndrome 2EnrichmentTGFBR12.30
24Histiocytoma, angiomatoid fibrousEnrichmentCREB12.30
25Neuronopathy, distal hereditary motor, autosomal dominant 3EnrichmentHSPB12.30
26Immunodeficiency 31cEnrichmentSTAT12.30
27Intellectual developmental disorder, autosomal dominant 48EnrichmentRAC12.30
28Loeys-dietz syndrome 4EnrichmentTGFB22.30
29Immune system diseaseEnrichmentCDC422.30
30Immunodeficiency 57 with autoinflammationEnrichmentRIPK12.30
31Wooly hair nevusEnrichmentHRAS2.30
32Familial thoracic aortic aneurysm and aortic dissectionEnrichmentTGFB2, TGFBR12.27
33Large congenital melanocytic nevusEnrichmentHRAS2.12
34High-grade b-cell lymphoma double-hit/triple-hitEnrichmentMYC2.12
35Loeys-dietz syndrome 1EnrichmentTGFBR12.12
36Frontometaphyseal dysplasiaEnrichmentMAP3K72.12
37Myxoid liposarcomaEnrichmentDDIT32.12
38SpermatocytomaEnrichmentHRAS2.12
39Melanoma of soft tissueEnrichmentCREB12.12
40Schimmelpenning-feuerstein-mims syndromeEnrichmentHRAS2.00
41Aortic aneurysmEnrichmentTGFBR12.00
42Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemiaEnrichmentCDC422.00
43Epidermolytic nevusEnrichmentHRAS2.00
44Neuronopathy, distal hereditary motor, autosomal dominant 2EnrichmentHSPB11.90
45Atrial septal defect 1EnrichmentTGFB21.83
46Inflammatory bowel disease 25, autosomal recessiveEnrichmentRIPK11.83
47Chronic mucocutaneous candidiasisEnrichmentSTAT11.83
48Il10-related early-onset inflammatory bowel diseaseEnrichmentRIPK11.83
49Classic ehlers-danlos syndromeEnrichmentTGFBR11.83
50Nevus, epidermalEnrichmentHRAS1.76
51Thyroid cancer, nonmedullary, 2EnrichmentHRAS1.76
52Noonan syndrome 3EnrichmentHRAS1.76
53Follicular thyroid carcinomaEnrichmentHRAS1.76
54Melanocytic nevus syndrome, congenitalEnrichmentHRAS1.70
55Neurodevelopmental disorder with dysmorphic facies and distal limb anomaliesEnrichmentRAC11.65
56Arteriovenous malformationEnrichmentHRAS1.65
57Myopathy, x-linked, with excessive autophagyEnrichmentHRAS1.61
58Pectus excavatumEnrichmentTGFBR11.56
59Immune deficiency diseaseEnrichmentRIPK11.56
6046,xy complete gonadal dysgenesisEnrichmentMAP3K11.56
61Lung non-small cell carcinomaEnrichmentHRAS1.56
62Lip and oral cavity carcinomaEnrichmentHRAS1.53
63PheochromocytomaEnrichmentMAX1.46
6446,xy partial gonadal dysgenesisEnrichmentMAP3K11.46
65Noonan syndrome and noonan-related syndromeEnrichmentHRAS1.43
66RhabdomyosarcomaEnrichmentHRAS1.40
67Ehlers-danlos syndromeEnrichmentTGFB21.33
68Hereditary paraganglioma-pheochromocytoma syndromesEnrichmentMAX1.29
69Noonan syndrome 1EnrichmentHRAS1.25
70Precursor t-cell acute lymphoblastic leukemiaEnrichmentMYC1.25
71Hydrops fetalis, nonimmuneEnrichmentHRAS1.20
72RasopathyEnrichmentHRAS1.20
73Bladder cancerEnrichmentHRAS1.15
74Differentiated thyroid carcinomaEnrichmentHRAS1.15
75Non-immune hydrops fetalisEnrichmentHRAS1.13
76Charcot-marie-tooth diseaseEnrichmentHSPB11.01
77Hereditary breast ovarian cancer syndromeEnrichmentRIPK10.89
78Breast cancerEnrichmentSHC10.76
79Ovarian cancerEnrichmentMAP3K10.65
80Inherited cancer-predisposing syndromeEnrichmentMAX0.55

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