Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3569
Gene Symbol: IL6
IL6 		0.010 AlteredExpression disease BEFREE Laryngomalacia could be an inflammatory disease due to 25(OH)-vitamin D deficiency as evidenced by the high level of IL-6. 30972761 2020
Entrez Id: 3553
Gene Symbol: IL1B
IL1B 		0.010 AlteredExpression disease BEFREE Presence and level of salivary pepsin was not significantly associated with need for surgical management, nor were the levels or presence of IL-1β or IL-8 significantly associated with presence or level of pepsin, diagnosis of laryngomalacia, or need for operative management. 31631681 2020
Entrez Id: 27086
Gene Symbol: FOXP1
FOXP1 		0.010 Biomarker disease BEFREE Although it is known that FOXP1 defects are related to abnormalities in vocal communication, FOXP1-associated laryngomalacia or vocal cord paralysis/immobilization cases have not been reported yet. 30579078 2019
Entrez Id: 80816
Gene Symbol: ASXL3
ASXL3 		0.100 CausalMutation disease CLINVAR Novel splicing mutation in the ASXL3 gene causing Bainbridge-Ropers syndrome. 27075689 2016
Entrez Id: 57492
Gene Symbol: ARID1B
ARID1B 		0.100 CausalMutation disease CLINVAR Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability. 26350204 2015
Entrez Id: 57492
Gene Symbol: ARID1B
ARID1B 		0.100 CausalMutation disease CLINVAR Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome. 22426309 2012
Entrez Id: 3239
Gene Symbol: HOXD13
HOXD13 		0.100 Biomarker disease HPO
Entrez Id: 27125
Gene Symbol: AFF4
AFF4 		0.100 Biomarker disease HPO
Entrez Id: 6239
Gene Symbol: RREB1
RREB1 		0.100 Biomarker disease HPO
Entrez Id: 1123
Gene Symbol: CHN1
CHN1 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 101929328
Gene Symbol: KCNMA1-AS1
KCNMA1-AS1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 374654
Gene Symbol: KIF7
KIF7 		0.100 Biomarker disease HPO
Entrez Id: 4285
Gene Symbol: MIPEP
MIPEP 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 1387
Gene Symbol: CREBBP
CREBBP 		0.100 Biomarker disease HPO
Entrez Id: 7486
Gene Symbol: WRN
WRN 		0.100 Biomarker disease HPO
Entrez Id: 23594
Gene Symbol: ORC6
ORC6 		0.100 Biomarker disease HPO
Entrez Id: 6926
Gene Symbol: TBX3
TBX3 		0.100 Biomarker disease HPO
Entrez Id: 219844
Gene Symbol: HYLS1
HYLS1 		0.100 Biomarker disease HPO
Entrez Id: 2812
Gene Symbol: GP1BB
GP1BB 		0.100 Biomarker disease HPO
Entrez Id: 91179
Gene Symbol: SCARF2
SCARF2 		0.100 Biomarker disease HPO
Entrez Id: 6134
Gene Symbol: RPL10
RPL10 		0.100 Biomarker disease HPO
Entrez Id: 3778
Gene Symbol: KCNMA1
KCNMA1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 4038
Gene Symbol: LRP4
LRP4 		0.100 Biomarker disease HPO
Entrez Id: 1312
Gene Symbol: COMT
COMT 		0.100 Biomarker disease HPO
Entrez Id: 4604
Gene Symbol: MYBPC1
MYBPC1 		0.100 GeneticVariation disease CLINVAR