Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
0.040 GeneticVariation group BEFREE Mutations in NIPBL are the most frequent cause of Cornelia de Lange syndrome (CdLS), a developmental disorder encompassing several neurological defects, including intellectual disability and seizures. 28041881 2017
Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
0.040 GeneticVariation group BEFREE Cornelia de Lange syndrome is a multisystemic developmental disorder mainly related to de novo heterozygous NIPBL mutation. 26701315 2016
Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
0.040 GeneticVariation group BEFREE Cornelia de Lange syndrome (CdLS) is a developmental disorder caused by mutations in NIPBL, a protein which has functionally been associated with the cohesin complex. 23760082 2013
Entrez Id: 25836
Gene Symbol: NIPBL
NIPBL
0.040 GeneticVariation group BEFREE Cornelia de Lange syndrome (CdLS) is a dominant multisystem developmental disorder and related to mutations of the NIPBL, SMC1A, and SMC3 genes. 22857006 2012