INHBB, inhibin subunit beta B, 3625

N. diseases: 22; N. variants: 0
Disease: Ectrodactyly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265554
Disease: Ectrodactyly
Ectrodactyly 		0.010 GeneticVariation disease BEFREE The breakpoint between INHBB and GLI2 coincides with a previously identified translocation breakpoint associated with ectrodactyly. 19223936 2009