Tacrolimus/Cyclosporine Pathway, Pharmacodynamics

No Pathway Network information available for Tacrolimus/Cyclosporine Pathway, Pharmacodynamics

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

Disorders associated with Tacrolimus/Cyclosporine Pathway, Pharmacodynamics SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Histiocytoid hemangiomaEnrichmentFOS, FOSB3.99
2Common variable immunodeficiencyEnrichmentNFKB1, NFKB23.67
3Multicentric carpotarsal osteolysis syndromeEnrichmentMAFB2.49
4Insulinomatosis and diabetes mellitusEnrichmentMAFA2.49
5Cardiospondylocarpofacial syndromeEnrichmentMAP3K72.49
6Cataract 21, multiple typesEnrichmentMAF2.49
746,xy sex reversal 6EnrichmentMAP3K12.49
8Frontometaphyseal dysplasia 2EnrichmentMAP3K72.49
9Immunodeficiency 92EnrichmentREL2.49
10Developmental and epileptic encephalopathy 91EnrichmentPPP3CA2.49
11Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual developmentEnrichmentPPP3CA2.49
12Enhanced s-cone syndrome 2EnrichmentNRL2.49
13Ayme-gripp syndromeEnrichmentMAF2.49
14Duane retraction syndrome 3 with or without deafnessEnrichmentMAFB2.49
15Deficiency in anterior pituitary function - variable immunodeficiency syndromeEnrichmentNFKB22.49
16Immunodeficiency 53EnrichmentRELB2.49
17Duane retraction syndrome 3EnrichmentMAFB2.49
18Aplasia cutis-enamel dysplasia syndromeEnrichmentFOSL22.49
19Duane retraction syndrome with congenital deafnessEnrichmentMAFB2.49
20Duane retraction syndrome 1EnrichmentMAFB2.19
21Camurati-engelmann disease 1EnrichmentTGFB12.19
22Phosphoenolpyruvate carboxykinase deficiency, mitochondrialEnrichmentNRL2.19
23Enhanced s-cone syndrome 1EnrichmentNRL2.19
24Developmental and epileptic encephalopathy 28EnrichmentMAF2.19
25Duane retraction syndrome 2EnrichmentMAFB2.19
26Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.19
27Immunodeficiency, common variable, 10EnrichmentNFKB22.19
28Spinocerebellar ataxia, autosomal recessive 12EnrichmentMAF2.19
29Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.19
30Inflammatory bowel disease, immunodeficiency, and encephalopathyEnrichmentTGFB12.19
31Rela fusion-positive ependymomaEnrichmentRELA2.19
32Camurati-engelmann diseaseEnrichmentTGFB12.19
33Enhanced s-cone syndromeEnrichmentNRL2.19
34Retinitis pigmentosa 27EnrichmentNRL2.19
35Joint contractures, osteochondromas, and b-cell lymphomaEnrichmentNFATC22.19
36Common variable immunodeficiency 12EnrichmentNFKB12.19
37Frontometaphyseal dysplasiaEnrichmentMAP3K72.01
38Duane retraction syndromeEnrichmentMAFB2.01
39Phosphoenolpyruvate carboxykinase deficiencyEnrichmentNRL2.01
40Immunodeficiency, common variable, 1EnrichmentNFKB21.89
41Congenital generalized lipodystrophyEnrichmentFOS1.89
42Congenital blue dot cataractEnrichmentMAF1.89
43Pseudomyogenic hemangioendotheliomaEnrichmentFOSB1.89
44Inflammatory bowel disease 25, autosomal recessiveEnrichmentTGFB11.71
45Il10-related early-onset inflammatory bowel diseaseEnrichmentTGFB11.71
46Breast cancerEnrichmentIL2, JUN1.61
47Cataract - microcornea syndromeEnrichmentMAF1.59
48Orofacial cleft 1EnrichmentMAFB1.54
49Cataract 30, multiple typesEnrichmentMAF1.50
50Ciliary dyskinesia, primary, 3EnrichmentNFKB11.50
5146,xy complete gonadal dysgenesisEnrichmentMAP3K11.45
5246,xy partial gonadal dysgenesisEnrichmentMAP3K11.35
53Cardiomyopathy, dilated, 1aEnrichmentNFATC21.18
54Developmental and epileptic encephalopathy 1EnrichmentMAF1.11
55Cystic fibrosisEnrichmentTGFB11.01
56Benign epilepsy with centrotemporal spikesEnrichmentMAF0.90
57Centralopathic epilepsyEnrichmentMAF0.88
58West syndromeEnrichmentMAF0.87
59Autosomal dominant non-syndromic intellectual disabilityEnrichmentPPP3CA0.82
60Undetermined early-onset epileptic encephalopathyEnrichmentPPP3CA0.78
61Ovarian cancerEnrichmentMAP3K10.55
62Retinitis pigmentosaEnrichmentNRL0.30
63Hereditary retinal dystrophyEnrichmentNRL0.21
64Fundus dystrophyEnrichmentNRL0.21

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