Exercise-induced circadian regulation

No Pathway Network information available for Exercise-induced circadian regulation

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

Disorders associated with Exercise-induced circadian regulation SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvementEnrichmentTUBB32.45
2Advanced sleep phase syndrome, familial, 1EnrichmentPER22.45
3Orofacial cleft 10EnrichmentSUMO12.45
4Renal hypodysplasia/aplasia 4EnrichmentGFRA12.45
5Delayed sleep phase disorderEnrichmentCRY12.45
6Onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndromeEnrichmentPIGF2.45
7Developmental and epileptic encephalopathy 83EnrichmentUGP22.45
8B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1)EnrichmentETV62.45
9Autosomal recessive spastic paraplegia type 71EnrichmentZFR2.45
105q31.3 microdeletion syndromeEnrichmentPURA2.45
11Polyvalvular heart disease syndromeEnrichmentTAB22.45
12Differentiated thyroid carcinomaEnrichmentETV6, NCOA42.33
13Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficultiesEnrichmentPURA2.15
14Immunodeficiency 72 with autoinflammation and lymphoproliferationEnrichmentNCKAP12.15
15Kala-azar 2EnrichmentGSTP12.15
16Hematologic cancerEnrichmentETV62.15
17Congenital mesoblastic nephromaEnrichmentETV62.15
18Angiocentric gliomaEnrichmentQKI2.15
19Cortical dysplasia, complex, with other brain malformations 1EnrichmentTUBB32.15
20Congenital heart defects, multiple types, 2EnrichmentTAB22.15
21FibrosarcomaEnrichmentETV62.15
22Pura-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutationEnrichmentPURA2.15
23Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndromeEnrichmentTAB22.15
24Immunodeficiency 72EnrichmentNCKAP12.15
25Pelvic organ prolapseEnrichmentTAB21.98
26Thrombocytopenia 5EnrichmentETV61.98
27Advanced sleep phase syndromeEnrichmentPER21.98
28Tubulinopathy-associated dysgyriaEnrichmentTUBB31.98
29Leptin deficiency or dysfunctionEnrichmentUCP31.85
30Chronic myelomonocytic leukemiaEnrichmentETV61.85
31Atrioventricular septal defectEnrichmentNR1D21.76
32Autosomal thrombocytopenia with normal plateletsEnrichmentETV61.76
33Primary hypereosinophilic syndromeEnrichmentETV61.76
34Myopathy, centronuclear, 1EnrichmentMYF61.68
35Congenital fibrosis of the extraocular musclesEnrichmentTUBB31.68
36Renal agenesis, bilateralEnrichmentGFRA11.50
37Migraine with or without aura 1EnrichmentTAB21.42
38Leukemia, acute lymphoblasticEnrichmentETV61.42
39Aortic valve disease 1EnrichmentTAB21.35
40Hermansky-pudlak syndrome 1EnrichmentETV61.26
41Patent foramen ovaleEnrichmentTAB21.21
42Diffuse large b-cell lymphomaEnrichmentETV61.19
43LissencephalyEnrichmentTUBB31.14
44Tooth agenesisEnrichmentSUMO11.12
45Cystic fibrosisEnrichmentGSTM30.97
46Leukemia, acute myeloidEnrichmentETV60.88
47ThrombocytopeniaEnrichmentETV60.80
48Body mass index quantitative trait locus 11EnrichmentUCP30.79
49Spastic ataxiaEnrichmentTUBB30.77
50Hereditary breast ovarian cancer syndromeEnrichmentHERPUD10.75
51Dilated cardiomyopathyEnrichmentTAB20.61
52Congenital nervous system abnormalityEnrichmentPURA0.50
53Nervous system diseaseEnrichmentPURA0.50

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