Role of phospholipids in phagocytosis

No Pathway Network information available for Role of phospholipids in phagocytosis

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

Disorders associated with Role of phospholipids in phagocytosis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Congenital lipomatous overgrowth, vascular malformations, and epidermal neviEnrichmentPIK3CA, PIK3R15.01
2Megalencephaly-capillary malformation-polymicrogyria syndromeEnrichmentPIK3CA, PIK3R24.71
3Severe combined immunodeficiencyEnrichmentCD247, CD3G2.78
4Anhidrosis, isolated, with normal sweat glandsEnrichmentITPR22.73
5MacrodactylyEnrichmentPIK3CA2.73
6Osteopetrosis and infantile neuroaxonal dystrophyEnrichmentPLA2G62.73
7Megalencephaly, autosomal dominantEnrichmentPIK3CA2.73
8Cowden syndrome 5EnrichmentPIK3CA2.73
9Cardiac valvular dysplasia 1EnrichmentPLD12.73
10Immunodeficiency 20EnrichmentFCGR3A2.73
11Autoimmune lymphoproliferative syndrome, type iiiEnrichmentPRKCD2.73
12Cerebral cavernous malformations 4EnrichmentPIK3CA2.73
13Immunodeficiency 82 with systemic inflammationEnrichmentSYK2.73
14Neurodegeneration with brain iron accumulation 2aEnrichmentPLA2G62.73
15Charcot-marie-tooth disease, demyelinating, type 1jEnrichmentITPR32.73
16Short syndromeEnrichmentPIK3R12.73
17Immune dysregulation, autoimmunity, and autoinflammationEnrichmentPLCG12.73
18Immunodeficiency 25EnrichmentCD2472.73
19Hemifacial myohyperplasiaEnrichmentPIK3CA2.73
20Parkinson disease 14, autosomal recessiveEnrichmentPLA2G62.73
21Capillary malformation of the lower lip, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowthEnrichmentPIK3CA2.73
22Neurodegeneration with brain iron accumulation 2bEnrichmentPLA2G62.73
23Immunodeficiency 36 with lymphoproliferationEnrichmentPIK3R12.73
24Autoinflammation, antibody deficiency, and immune dysregulationEnrichmentPLCG22.73
25Agammaglobulinemia 7, autosomal recessiveEnrichmentPIK3R12.73
26Familial cold autoinflammatory syndrome 3EnrichmentPLCG22.73
27Segmental progressive overgrowth syndrome with fibroadipose hyperplasiaEnrichmentPIK3CA2.73
28HypospadiasEnrichmentPIK3CA2.73
29Immunodeficiency 133 with ectodermal dysplasia with or without peripheral neuropathyEnrichmentITPR32.73
30ColitisEnrichmentSYK2.73
31Systemic lupus erythematosus 18EnrichmentPLD42.73
32Rare venous malformationEnrichmentPIK3CA2.73
33Diaphragmatic eventrationEnrichmentPIK3CA2.73
34Pik3ca-related overgrowth spectrumEnrichmentPIK3CA2.73
35Rare combined vascular malformationEnrichmentPIK3CA2.73
36Cavernous lymphangiomaEnrichmentPIK3CA2.73
37Pik3ca-related overgrowth syndromeEnrichmentPIK3CA2.73
38Hemihyperplasia-multiple lipomatosis syndromeEnrichmentPIK3CA2.73
39Eccrine angiomatous hamartomaEnrichmentPIK3CA2.73
40Macrodactyly of toeEnrichmentPIK3CA2.73
41Spinocerebellar ataxia 29EnrichmentITPR12.43
42Charcot-marie-tooth disease, demyelinating, type 4fEnrichmentPLD32.43
43Keratosis, seborrheicEnrichmentPIK3CA2.43
44Noonan syndrome 8EnrichmentPIK3CA2.43
45Spinocerebellar ataxia 46EnrichmentPLD32.43
46Rosette-forming glioneuronal tumorEnrichmentPIK3CA2.43
47Immunodeficiency 17EnrichmentCD3G2.43
48Charcot-marie-tooth disease type 4fEnrichmentPLD32.43
49ArthritisEnrichmentSYK2.43
50Infantile osteopetrosis with neuroaxonal dysplasiaEnrichmentPLA2G62.43
51Spastic ataxiaEnrichmentITPR1, PLA2G62.37
52Gillespie syndromeEnrichmentITPR12.26
53Pompe disease, infantile-onsetEnrichmentPIK3CA2.26
54Immunodeficiency 14a with lymphoproliferation, autosomal dominantEnrichmentPIK3R12.26
55Immunodeficiency 14EnrichmentPIK3R12.26
56T-b+ severe combined immunodeficiency due to cd3delta/cd3epsilon/cd3zetaEnrichmentCD2472.26
57KeratoacanthomaEnrichmentPIK3CA2.26
58Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1EnrichmentPIK3R22.13
59Spinocerebellar ataxia 15EnrichmentITPR12.13
60Cerebrovascular diseaseEnrichmentPIK3CA2.13
61Familial cerebral cavernous malformationsEnrichmentPIK3CA2.13
62Capillary malformations, congenitalEnrichmentPIK3CA2.04
63HemimegalencephalyEnrichmentPIK3CA2.04
64Klippel-trenaunay-weber syndromeEnrichmentPIK3CA1.96
65Cowden syndrome 1EnrichmentPIK3CA1.96
66Hemihyperplasia, isolatedEnrichmentPIK3CA1.96
67Spinocerebellar ataxia, autosomal recessive 16EnrichmentITPR11.96
68Breast adenocarcinomaEnrichmentPIK3CA1.96
69Lung squamous cell carcinomaEnrichmentPIK3CA1.96
70Colorectal cancerEnrichmentPIK3CA, PIK3R11.96
71Nevus, epidermalEnrichmentPIK3CA1.89
72Capillary malformation-arteriovenous malformation 1EnrichmentPIK3CA1.89
73Gallbladder cancerEnrichmentPIK3CA1.89
74Oligoarticular juvenile idiopathic arthritisEnrichmentCD2471.89
75Overgrowth syndromeEnrichmentPIK3R11.89
76Rheumatoid factor-negative juvenile idiopathic arthritisEnrichmentCD2471.89
77Arteriovenous malformationEnrichmentPIK3CA1.78
78Adult hepatocellular carcinomaEnrichmentPIK3CA1.78
79Cowden syndromeEnrichmentPIK3CA1.78
80Myopathy, x-linked, with excessive autophagyEnrichmentPIK3CA1.74
81Neurodegeneration with brain iron accumulationEnrichmentPLA2G61.74
82Autosomal non-syndromic agammaglobulinemiaEnrichmentPIK3R11.74
83Immune deficiency diseaseEnrichmentSYK1.70
84Lung non-small cell carcinomaEnrichmentPIK3CA1.70
85MeningiomaEnrichmentPIK3CA1.66
86Lip and oral cavity carcinomaEnrichmentPIK3CA1.66
87Congenital long qt syndromeEnrichmentITPR31.66
88Nk-cell enteropathyEnrichmentPIK3CB1.63
89Multiple sclerosisEnrichmentITPR11.59
90Anterior segment dysgenesisEnrichmentITPR11.56
91Lynch syndromeEnrichmentPIK3CA1.56
92Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delayEnrichmentPLA2G61.54
93Charcot-marie-tooth disease type 4EnrichmentPLD31.49
94Endometrial cancerEnrichmentPIK3CA1.42
95Hepatocellular carcinomaEnrichmentPIK3CA1.40
96MalariaEnrichmentFCGR2A1.38
97Bladder cancerEnrichmentPIK3CA1.28
98Prostate cancerEnrichmentPIK3CA1.28
99Long qt syndrome 1EnrichmentITPR31.27
100Lung cancerEnrichmentPIK3CA1.24
101Cystic fibrosisEnrichmentFCGR2A1.24
102Systemic lupus erythematosusEnrichmentFCGR2A1.16
103Charcot-marie-tooth diseaseEnrichmentPLD31.14
104Gastric cancerEnrichmentPIK3CA1.12
105Hereditary breast carcinomaEnrichmentPIK3CA1.11
106HypertelorismEnrichmentPIK3CA1.04
107Myeloma, multipleEnrichmentPIK3R21.01
108Breast cancerEnrichmentPIK3CA0.89
109Ovarian cancerEnrichmentPIK3CA0.77
110Congenital nervous system abnormalityEnrichmentPLA2G60.75
111Nervous system diseaseEnrichmentPLA2G60.75
112MicrocephalyEnrichmentPLA2G60.69

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