WNT10B, Wnt family member 10B, 7480

N. diseases: 90; N. variants: 23
Disease: Ectrodactyly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265554
Disease: Ectrodactyly
Ectrodactyly 		0.300 GermlineCausalMutation disease ORPHANET Homozygous nonsense mutation in WNT10B and sporadic split-hand/foot malformation (SHFM) with autosomal recessive inheritance. 20635353 2010
CUI: C0265554
Disease: Ectrodactyly
Ectrodactyly 		0.300 GermlineCausalMutation disease ORPHANET Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation. 18515319 2008