Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1636
Gene Symbol: ACE
ACE
0.010 Biomarker disease BEFREE Moreover, the role of ACE inhibition has been explored in the treatment of Cardiovascular Autonomic Neuropathy. 31109280 2020
Entrez Id: 213
Gene Symbol: ALB
ALB
0.030 Biomarker disease BEFREE Glycated albumin and its variability as an indicator of cardiovascular autonomic neuropathy development in type 2 diabetic patients. 29017498 2017
Entrez Id: 213
Gene Symbol: ALB
ALB
0.030 Biomarker disease BEFREE The distribution of DR3 and DR4 risk alleles was not associated with cardiovascular autonomic neuropathy both in patients with normal albumin excretion rate and microalbuminuria (1.6 vs 2.1; p = 0.21). 27036319 2016
Entrez Id: 213
Gene Symbol: ALB
ALB
0.030 Biomarker disease BEFREE Autonomic neuropathy in nondiabetic offspring of type 2 diabetic subjects is associated with urinary albumin excretion rate and 24-h ambulatory blood pressure: the Fredericia Study. 11246884 2001
Entrez Id: 335
Gene Symbol: APOA1
APOA1
0.010 Biomarker disease BEFREE Serum apolipoprotein A-1 concentrations and the prevalence of cardiovascular autonomic neuropathy in individuals with type 2 diabetes. 29453140 2018
Entrez Id: 1437
Gene Symbol: CSF2
CSF2
0.010 Biomarker disease BEFREE Here, we describe two patients complaining of autonomic symptoms in whom a post-ganglionic autonomic neuropathy has been demonstrated in association with significantly elevated serum and CSF GAD-Abs levels. 27913968 2017
Entrez Id: 64858
Gene Symbol: DCLRE1B
DCLRE1B
0.010 Biomarker disease BEFREE The effect of the RNAi therapeutic, patisiran, on autonomic neuropathy manifestations in patients with hATTR amyloidosis with polyneuropathy in the phase III APOLLO study is reported. 31728713 2020
Entrez Id: 1786
Gene Symbol: DNMT1
DNMT1
0.010 GeneticVariation disease BEFREE The fact that heterozygous mutations in DNMT1 are associated with hereditary sensory autonomic neuropathy provides plausibility to the present finding. 30548403 2019
Entrez Id: 667
Gene Symbol: DST
DST
0.010 AlteredExpression disease BEFREE Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI. 24381311 2014
Entrez Id: 8518
Gene Symbol: ELP1
ELP1
0.010 GeneticVariation disease BEFREE We recently identified a mutation in the I-kappa B kinase associated protein (IKBKAP) gene as the major cause of familial dysautonomia (FD), a recessive sensory and autonomic neuropathy. 12577200 2003
Entrez Id: 2056
Gene Symbol: EPO
EPO
0.010 Biomarker disease BEFREE DKD-related anemia developed earlier and was more severe than non-DKD-related anemia based on more complicated mechanisms, including greater bleeding tendency associated with antiplatelet effect, less O2 sensing due to autonomic neuropathy or renin-angiotensin-aldosterone system inhibitor use, inhibitory effect of inflammatory cytokines, urinary loss of erythropoietin (EPO), and poor response to EPO. 31453863 2019
Entrez Id: 2191
Gene Symbol: FAP
FAP
0.010 GeneticVariation disease BEFREE Hereditary ATTR (ATTRm) amyloidosis (also called transthyretin-type familial amyloid polyneuropathy [ATTR-FAP]) is an autosomal-dominant, adult-onset, rare systemic disorder predominantly characterized by irreversible, progressive, and persistent peripheral nerve damage.TTR gene mutations (e.g. replacement of valine with methionine at position 30 [Val30Met (p.Val50Met)]) lead to destabilization and dissociation of TTR tetramers into variant TTR monomers, which form amyloid fibrils that deposit in peripheral nerves and various organs, giving rise to peripheral and autonomic neuropathy and several non-disease specific symptoms.Phenotypic and genetic variability and non-disease-specific symptoms often delay diagnosis and lead to misdiagnosis. 29343286 2018
Entrez Id: 28982
Gene Symbol: FLVCR1
FLVCR1
0.010 GeneticVariation disease BEFREE Posterior column ataxia with retinitis pigmentosa coexisting with sensory-autonomic neuropathy and leukemia due to the homozygous p.Pro221Ser FLVCR1 mutation. 28766925 2017
Entrez Id: 2571
Gene Symbol: GAD1
GAD1
0.010 AlteredExpression disease BEFREE Here, we describe two patients complaining of autonomic symptoms in whom a post-ganglionic autonomic neuropathy has been demonstrated in association with significantly elevated serum and CSF GAD-Abs levels. 27913968 2017
Entrez Id: 64083
Gene Symbol: GOLPH3
GOLPH3
0.010 GeneticVariation disease BEFREE Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy. 19838196 2009
Entrez Id: 2879
Gene Symbol: GPX4
GPX4
0.010 GeneticVariation disease BEFREE Glutathione peroxidase 4 functional variant rs713041 modulates the risk for cardiovascular autonomic neuropathy in individuals with type 1 diabetes. 30599773 2019
Entrez Id: 373156
Gene Symbol: GSTK1
GSTK1
0.010 GeneticVariation disease BEFREE The aim of the study was to compare the prevalence of GST T1/M1 gene polymorphisms between diabetic adolescents with (CAN+) and without (CAN-) cardiovascular autonomic neuropathy. 23021798 2013
Entrez Id: 27306
Gene Symbol: HPGDS
HPGDS
0.010 GeneticVariation disease BEFREE The association between glutathione S-transferase T1 and M1 gene polymorphisms and cardiovascular autonomic neuropathy in Slovak adolescents with type 1 diabetes mellitus. 23021798 2013
Entrez Id: 3258
Gene Symbol: HPT
HPT
0.010 Biomarker disease BEFREE Cardiovascular Autonomic Neuropathy as a New Complication of Postsurgical Chronic Hypoparathyroidism. 30395692 2019
Entrez Id: 547
Gene Symbol: KIF1A
KIF1A
0.020 GeneticVariation disease BEFREE Recessive mutations in KIF1A were previously described in families with spastic paraparesis or sensory and autonomic neuropathy type-2. 25265257 2015
Entrez Id: 547
Gene Symbol: KIF1A
KIF1A
0.020 GeneticVariation disease BEFREE Autosomal recessive <i>KIF1A</i> missense mutations cause hereditary spastic paraplegia (HSP) type SPG30, while recessive truncations lead to sensory and autonomic neuropathy (HSN2C) and many de novo missense mutations are associated with cognitive impairment. 29159194 2017
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
0.010 Biomarker disease BEFREE Here, we describe two patients complaining of autonomic symptoms in whom a post-ganglionic autonomic neuropathy has been demonstrated in association with significantly elevated serum and CSF GAD-Abs levels. 27913968 2017
Entrez Id: 693203
Gene Symbol: MIR618
MIR618
0.010 AlteredExpression disease BEFREE <b>Conclusions:</b> In this cohort of type 1 diabetes individuals, serum miR-518d-3p and miR-618 were upregulated in those with diabetes kidney disease, diabetes retinopathy, peripheral neuropathy, and cardiovascular autonomic neuropathy in comparison to individuals with no microvascular complications. 31249556 2019
Entrez Id: 4803
Gene Symbol: NGF
NGF
0.020 GeneticVariation disease BEFREE Taking pain out of NGF: a "painless" NGF mutant, linked to hereditary sensory autonomic neuropathy type V, with full neurotrophic activity. 21387003 2011
Entrez Id: 4803
Gene Symbol: NGF
NGF
0.020 GeneticVariation disease BEFREE In this study we exploit forms of NGF, mutated at residue R100, inspired by the human genetic disease HSAN V (Hereditary Sensory Autonomic Neuropathy Type V), which would allow increasing the dose of NGF without triggering pain. 22666365 2012