Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 GeneticVariation 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 GeneticVariation 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 GeneticVariation 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 GeneticVariation 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 GeneticVariation 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 GeneticVariation 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 GeneticVariation 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker 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