PKNOX2, PBX/knotted 1 homeobox 2, 63876

N. diseases: 19; N. variants: 6
Disease: Hydrolethalus syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931104
Disease: Hydrolethalus syndrome
Hydrolethalus syndrome 		0.010 GeneticVariation disease BEFREE The linkage disequilibrium (LD) and haplotype analyses of single nucleotide polymorphism (SNP) markers helped to further restrict the HLS locus to 476 kb between genes PKNOX2 and DDX25. 15843405 2005