Selenium Metabolism and Selenoproteins

No Pathway Network information available for Selenium Metabolism and Selenoproteins

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

Disorders associated with Selenium Metabolism and Selenoproteins SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Spondylometaphyseal dysplasia, sedaghatian typeEnrichmentGPX42.56
2Glucocorticoid deficiency 5EnrichmentTXNRD22.56
3Glutathione peroxidase deficiencyEnrichmentGPX12.56
4Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndromeEnrichmentSARS22.56
5Spastic paraplegia 81, autosomal recessiveEnrichmentSELENOI2.56
6Thyroid hormone metabolism, abnormal, 2EnrichmentDIO12.56
7Extraoral halitosis due to methanethiol oxidase deficiencyEnrichmentSELENBP12.56
8Immunodeficiency, common variable, 12, with autoimmunityEnrichmentNFKB12.26
9Autoinflammatory disease, familial, behcet-like 3EnrichmentRELA2.26
10Rela fusion-positive ependymomaEnrichmentRELA2.26
11Common variable immunodeficiency 12EnrichmentNFKB12.26
12Microcephaly, postnatal progressive, with seizures and brain atrophyEnrichmentEEFSEC2.09
13Neurodevelopmental disorder with progressive spasticity and brain abnormalitiesEnrichmentEEFSEC2.09
14KyphosisEnrichmentSEPSECS2.09
15Congenital generalized lipodystrophyEnrichmentFOS1.96
16Congenital myopathy 3 with rigid spineEnrichmentSELENON1.87
17Pontocerebellar hypoplasia, type 2dEnrichmentSEPSECS1.87
18Spastic diplegiaEnrichmentSEPSECS1.87
19Histiocytoid hemangiomaEnrichmentFOS1.87
20Familial glucocorticoid deficiencyEnrichmentTXNRD21.87
21Autosomal recessive intellectual developmental disorderEnrichmentEEFSEC1.79
22Pontocerebellar hypoplasia, type 2eEnrichmentSEPSECS1.72
23Common variable immunodeficiencyEnrichmentNFKB11.72
24Ciliary dyskinesia, primary, 3EnrichmentNFKB11.57
25Congenital myopathy 4a, autosomal dominantEnrichmentSELENON1.40
26Pontocerebellar hypoplasiaEnrichmentSEPSECS1.32
27Muscular dystrophyEnrichmentSELENON1.20
28Distal arthrogryposisEnrichmentSEPSECS0.96
29Spastic ataxiaEnrichmentSEPSECS0.87
30Familial isolated dilated cardiomyopathyEnrichmentTXNRD20.87
31Autosomal recessive non-syndromic intellectual disabilityEnrichmentEEFSEC0.83
32Breast cancerEnrichmentJUN0.73

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