Gene: MYH3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4621
Gene Symbol: MYH3
MYH3 		0.120 GeneticVariation phenotype BEFREE Mutations in embryonic MyHC (MYH3) and perinatal MyHC (MYH8) are associated with distal arthrogryposis syndromes with no or minor muscle weakness. 19181095 2008
Entrez Id: 4621
Gene Symbol: MYH3
MYH3 		0.120 GeneticVariation phenotype BEFREE Mutations in embryonic MyHC (MYH3) and perinatal MyHC (MYH8), which are myosin isoforms expressed during muscle development, are associated with distal arthrogryposis syndromes with no or minor muscle weakness. 17434305 2007
Entrez Id: 4621
Gene Symbol: MYH3
MYH3 		0.120 Biomarker phenotype HPO