MYL3, myosin light chain 3, 4634

N. diseases: 37; N. variants: 17
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8 ×
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C1837471
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 1 8 0.700 strong 1.000 9 8 1996 2019