MYH7B, myosin heavy chain 7B, 57644

N. diseases: 18; N. variants: 20
Disease: Congenital Fiber Type Disproportion ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0546264
Disease: Congenital Fiber Type Disproportion
Congenital Fiber Type Disproportion 		0.010 GeneticVariation disease BEFREE Mutation in MYH7B causes a classical LVNC phenotype, whereas mutation in ITGA7 causes CFTD. 23800289 2013