WNT5B, Wnt family member 5B, 81029

N. diseases: 39; N. variants: 6
Disease: Goldenhar Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265240
Disease: Goldenhar Syndrome
Goldenhar Syndrome 		0.010 Biomarker disease BEFREE 2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate gene. 19733267 2010