Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 30813
Gene Symbol: VSX1
VSX1
0.320 Biomarker group BEFREE GCPS is mainly characterised by craniofacial abnormalities (macrocephaly/prominent forehead, hypertelorism) and limb malformations, such as PPD-IV, syndactyly and postaxial polydactyly type A or B (PAPA/B). 22903559 2012
Entrez Id: 30813
Gene Symbol: VSX1
VSX1
0.320 Biomarker group CTD_human VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells. 15051220 2004
Entrez Id: 30813
Gene Symbol: VSX1
VSX1
0.320 GeneticVariation group BEFREE VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells. 15051220 2004