NHLH1, nescient helix-loop-helix 1, 4807

N. diseases: 33; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0302142
Disease: Deformity
Deformity
0.070 Biomarker group 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
CUI: C0302142
Disease: Deformity
Deformity
0.070 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
CUI: C0302142
Disease: Deformity
Deformity
0.070 Biomarker group BEFREE Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a structural craniofacial malformation featured by isolated orofacial abnormalities. 27734840 2017
CUI: C0302142
Disease: Deformity
Deformity
0.070 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
CUI: C0302142
Disease: Deformity
Deformity
0.070 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
CUI: C0302142
Disease: Deformity
Deformity
0.070 GeneticVariation group BEFREE Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common structural malformation with a complex and multifactorial aetiology. 24606907 2014
CUI: C0302142
Disease: Deformity
Deformity
0.070 Biomarker group BEFREE Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is one of the most common craniofacial malformation in humans. 23166094 2012