INHBB, inhibin subunit beta B, 3625

N. diseases: 22; N. variants: 0
Disease: Split hand foot deformity 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2931019
Disease: Split hand foot deformity 1
Split hand foot deformity 1 		0.010 GeneticVariation disease BEFREE The breakpoint between INHBB and GLI2 coincides with a previously identified translocation breakpoint associated with ectrodactyly. 19223936 2009