Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common orofacial congenital anomaly. 28906376 2017
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a prevalent, complex congenital malformation. 27350171 2017
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 GeneticVariation group BEFREE Non-syndromic cleft lip with or without cleft palate (NSCL/P) are the most common human congenital birth defects with a complex etiology. 30024657 2018
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Orofacial clefts (OFCs), including nonsyndromic cleft lip with or without cleft palate (NSCL/P), are common birth defects. 28762674 2017
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is the most common craniofacial birth defect in humans, affecting 1 in 700 live births. 28019042 2017
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Non‑syndromic cleft lip with or without cleft palate (NSCL/P) is a common congenital deformity, often associated with missing or deformed teeth. 23921572 2013
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect which is strongly associated with genetic factors. 25220223 2015
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 GeneticVariation group BEFREE To understand the genetic basis of nonsyndromic cleft lip with or without cleft palate (NSCL/P) susceptibility, a complex and highly prevalent congenital malformation, we searched for genetic variants with a regulatory role in a disease-related tissue, the lip muscle (orbicularis oris muscle [OOM]), of affected individuals. 29053389 2018
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 GeneticVariation group BEFREE Our study provided additional understanding of the genetic etiology of NSCL/P and underlined the importance of considering gene-gene interaction in the etiology of this common craniofacial malformation. 29341488 2018
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect. 26505415 2015
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a common craniofacial birth defect that has a complex etiology. 27154735 2016
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 GeneticVariation group BEFREE Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is one of the most common congenital malformations and a susceptibility locus on chromosome 8q24 has been replicated as a genetic risk factor for NSCL/P in patients of European and Asian descent. 22044123 2012
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 GeneticVariation group BEFREE Non-syndromic cleft lip with or without cleft palate (NSCL/P) is the most common craniofacial malformation, with an incidence of about 1/700 live births, although variable according to ethnicity. 24942095 2014
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect with a complex and heterogeneous etiology. 28402597 2017
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect with complex etiology reflecting the action of multiple genetic and environmental factors. 23008150 2012
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Non-syndromic cleft lip with or without palate (NSCL/P) is one of the most common human birth defects, it results from multiple genetic and environmental risk factors. 30048854 2018
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Nonsyndromic cleft lip and/or palate (NSCL/P) is a prevalent birth defect of complex etiology. 28817352 2017
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a common congenital malformation associated with genetic and environmental risk factors. 22522387 2012
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 GeneticVariation group BEFREE In combination with results from our previous study using the same sample, our data suggest that the majority of the known NSCL/P susceptibility regions identified to date also confer risk for this malformation in the Mesoamerican population. 24382704 2014
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE In India, as in other parts of the world, nonsyndromic cleft lip with or without cleft palate (NSCL +/- P) is a highly prevalent birth defect, its incidence in males being twice that in females. 23385809 2013
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is one of the most common of all birth defects. 20564431 2010
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect. 30848863 2019
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 GeneticVariation group BEFREE Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is the most common orofacial birth defect with a wide range prevalence among different populations. 23679094 2013
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect of complex etiology. 25163644 2014
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
0.100 Biomarker group BEFREE Non-syndromic cleft lip/palate (NSCL/P) is a complex, frequent congenital malformation, determined by the interplay between genetic and environmental factors during embryonic development. 23776525 2013