Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4170
Gene Symbol: MCL1
MCL1
0.100 GeneticVariation group BEFREE Survey of suspected dysphagia prevalence in home-dwelling older people using the 10-Item Eating Assessment Tool (EAT-10). 30673750 2019
Entrez Id: 4170
Gene Symbol: MCL1
MCL1
0.100 GeneticVariation group BEFREE After adjusting for age, gender and ethnicity, the study identified [prevalence ratio (95% confidence interval)] high dysphagia risk [EAT-10 score: 0.98 (0.97-0.99)], low body mass index [kg/m<sup>2</sup>: 1.02 (1.02-1.03)], low muscle strength [hand grip strength, kg: 1.01 (1.00-1.02)] and decline in cognition [MoCA score: 1.01 (1.00-1.02)] as significant predictors of malnutrition risk in older adults at hospital admission. 29562879 2018
Entrez Id: 4170
Gene Symbol: MCL1
MCL1
0.100 GeneticVariation group BEFREE There was no significant difference in the prevalence of phonatory and dysphagia symptoms using VHI-10 and EAT-10 questionnaires between subjects with hypovitaminosis D and those with normal serum vitamin D levels. 30982641 2019
Entrez Id: 1778
Gene Symbol: DYNC1H1
DYNC1H1
0.100 GeneticVariation group CLINVAR
Entrez Id: 8506
Gene Symbol: CNTNAP1
CNTNAP1
0.100 GeneticVariation group CLINVAR Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy. 27668699 2017
Entrez Id: 9091
Gene Symbol: PIGQ
PIGQ
0.100 GeneticVariation group CLINVAR
Entrez Id: 4170
Gene Symbol: MCL1
MCL1
0.100 GeneticVariation group BEFREE Dysphagia was evaluated with the Eating Assessment Tool-10 (EAT-10), and the measurement of Maximal Isometric Tongue Pressure (MITP) and tongue endurance (Iowa Oral Performance Instrument-IOPI). 30579082 2019
Entrez Id: 4170
Gene Symbol: MCL1
MCL1
0.100 GeneticVariation group BEFREE The Eating Assessment Tool-10 (EAT-10) represents a validated, easy to administer patient report dysphagia severity scale. 27538876 2017
Entrez Id: 4170
Gene Symbol: MCL1
MCL1
0.100 GeneticVariation group BEFREE Responsiveness of the EAT-10 to Clinical Change in Head and Neck Cancer Patients with Dysphagia. 31032643 2019
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
0.100 GeneticVariation group CLINVAR
Entrez Id: 4170
Gene Symbol: MCL1
MCL1
0.100 GeneticVariation group BEFREE Preoperative and postoperative reflux symptomatology was subjectively measured with the Reflux Symptom Index (RSI), and dysphagia symptomatology was measured with the Eating Assessment Tool 10 (EAT-10). 27049450 2017
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
0.100 GeneticVariation group CLINVAR
Entrez Id: 6647
Gene Symbol: SOD1
SOD1
0.040 GeneticVariation group BEFREE In this observational population-based, registry study, we enrolled patients with newly- diagnosed ALS, according to the El Escorial revised criteria, who were resident in the Emilia Romagna Region, and who developed severe dysphagia needing enteral nutritional support. 28076984 2017
Entrez Id: 6647
Gene Symbol: SOD1
SOD1
0.040 GeneticVariation group BEFREE We recently established that the SOD1-G93A transgenic mouse is a suitable model for oral-stage dysphagia in amyotrophic lateral sclerosis (ALS). 19495873 2010
Entrez Id: 627
Gene Symbol: BDNF
BDNF
0.030 GeneticVariation group BEFREE The COMT polymorphism rs165599 and the BDNF polymorphism rs10835211 were found to predict dysphagia and have an interactive effect (p = 0.028), which varied according to the carrier status of the other. 26073434 2015
Entrez Id: 213
Gene Symbol: ALB
ALB
0.030 GeneticVariation group BEFREE The Access and No-Access cohorts had similar reported dysphagia (86% vs 75.5%, respectively; P = .2) and mean preesophagectomy serum albumin (3.9 vs 4 gm/dL, respectively; P = .2). 29198770 2018
Entrez Id: 1401
Gene Symbol: CRP
CRP
0.030 GeneticVariation group BEFREE The most significant predictors of ICU admission were lower third molar involvement (P = .026), dysphagia (P = .020), and C-reactive protein (CRP) levels exceeding 150 mg/L (P = .039). 29958865 2018
Entrez Id: 650
Gene Symbol: BMP2
BMP2
0.020 GeneticVariation group BEFREE Female gender, the use of anterior cervical plate, more than 1 surgical level, the upper surgical level at C3/4, and the use of rhBMP-2 are the risk factors for dysphagia following anterior cervical spinal surgery. 28272237 2017
Entrez Id: 3483
Gene Symbol: IGFALS
IGFALS
0.020 GeneticVariation group BEFREE In this observational population-based, registry study, we enrolled patients with newly- diagnosed ALS, according to the El Escorial revised criteria, who were resident in the Emilia Romagna Region, and who developed severe dysphagia needing enteral nutritional support. 28076984 2017
Entrez Id: 23451
Gene Symbol: SF3B1
SF3B1
0.010 GeneticVariation group BEFREE Dysphagia was identified with SCOPA-AUT question 1 (answer regularly) and was assessed with MDS-UPDRS Part-II, Item 2.3 (Chewing and Swallowing). 31344030 2019
Entrez Id: 54790
Gene Symbol: TET2
TET2
0.010 GeneticVariation group BEFREE Dysphagia was identified with SCOPA-AUT question 1 (answer regularly) and was assessed with MDS-UPDRS Part-II, Item 2.3 (Chewing and Swallowing). 31344030 2019
Entrez Id: 4907
Gene Symbol: NT5E
NT5E
0.010 GeneticVariation group BEFREE Medically Unexplained Oropharyngeal Dysphagia at the University Hospital ENT Outpatient Clinic for Dysphagia: A Cross-Sectional Cohort Study. 29872993 2019
Entrez Id: 5083
Gene Symbol: PAX9
PAX9
0.010 GeneticVariation group BEFREE Haploinsufficiency of the PAX9 gene might be expected to cause some of the developmental defects and the dysphagia. 10204852 1999
Entrez Id: 8518
Gene Symbol: ELP1
ELP1
0.010 GeneticVariation group BEFREE Dysphagia was the only symptom which differentiated patients with severe (14/16) or mild ELP (8/18) from patients without ELP (1/18). 31608788 2019
Entrez Id: 1950
Gene Symbol: EGF
EGF
0.010 GeneticVariation group BEFREE Mutations in the multiple epidermal growth factor-like domains 10 (MEGF10: NM_032446.2) gene are known to cause early-onset myopathy characterized by areflexia, respiratory distress, and dysphagia (EMARDD: OMIM 614399), and a milder phenotype of minicore myopathy. 27460346 2016