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/palate (NSCL/P) is a common congenital defect in Mexico. 24460828

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 one of the most common of all congenital malformations and has a multifactorial etiology. 22984993

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 a common congenital malformation worldwide, with complex etiology. 29211286

2018

Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker BEFREE Our observation that the impact of genetic variants on NSCL/P risk differs for males and females may further our understanding of the genetic architecture of NSCL/P and the sex differences underlying clefts and other birth defects. 30277614

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 among the most common congenital malformations. 26449438

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 group of common human birth defects with complex etiology. 28425186

2017

Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker BEFREE The GREM1 is involved in the etiology of NSCL±P in the Brazilian population and reveal that the interaction between GREM1 and NTN1 may be related with the pathogenesis of this common craniofacial malformation. 30402937

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 a common birth defect with a complex genetic architecture. 30273098

2019

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 birth defect for which several genes susceptibility genes been proposed. 29694940

2018

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 structural craniofacial malformation featured by isolated orofacial abnormalities. 27734840

2017

Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker BEFREE NSCL/P is a common congenital defect and gene-environmental factors involve in this disorder. 25716564

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) are common birth defects with a complex etiology. 23940636

2013

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 anomalies, with a complex and still not fully understood etiology. 22887353

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 one of the most common birth defects and has a multifactorial etiology that includes both genetic and environmental components. 19320731

2009

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 craniofacial malformation in humans. 23166094

2012

Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker BEFREE The non-syndromic cleft lip and/or palate (NSCL/P) is a common birth defect caused by a combination of genetic and environmental factors. 28096450

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 one of common birth defects in China, with genetic and environmental components contributing to the etiology. 30769929

2019

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 craniofacial birth defect, the risk of which is influenced from multiple genetic loci. 31132300

2019

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 congenital anomalies, and has a multifactorial etiology involving both environmental and genetic factors. 23081944

2012

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 among live births, and depends on race and ethnic background. 28151848

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), the most common type of orofacial clefting, is one of the most frequent congenital defects. 24038802

2013

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 craniofacial birth defect, characterised by an incomplete separation between nasal and oral cavities without any other congenital anomaly in humans. 25953455

2015

Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 Biomarker BEFREE These findings may reflect the presence of a genomic region containing potential causal variants interacting in the etiology of NSCL/P and may contribute to disentangling the complex etiology of this birth defect. 28133786

2017

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, exhibiting variable prevalence around the world, often attributed to ethnic and environmental differences. 26198054

2015

Entrez Id: 4807
Gene Symbol: NHLH1
NHLH1
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.100 GeneticVariation BEFREE The isolated type of orofacial cleft, termed non-syndromic cleft lip with or without cleft palate (NSCL/P), is the second most common birth defect in China, with Asians having the highest incidence in the world. 30578914

2018