Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2
0.410 Biomarker group CTD_human Neural crest-specific removal of Zfhx1b in mouse leads to a wide range of neurocristopathies reminiscent of Mowat-Wilson syndrome. 17478475 2007
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2
0.410 GeneticVariation group BEFREE Genotype-phenotype analysis confirmed that ZFHX1B deletions and stop mutations result in a recognizable facial dysmorphism with associated severe mental retardation and variable malformations such as Hirschsprung disease and congenital heart defects. 16053902 2005
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2
0.410 Biomarker group HPO