Gene: MYOT ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9499
Gene Symbol: MYOT
MYOT 		0.310 Biomarker phenotype CTD_human Mutations in myotilin cause myofibrillar myopathy. 15111675 2004
Entrez Id: 9499
Gene Symbol: MYOT
MYOT 		0.310 GeneticVariation phenotype BEFREE Limb-girdle muscular dystrophy 1A (LGMD1A [MIM 159000]) is an autosomal dominant form of muscular dystrophy characterized by adult onset of proximal weakness progressing to distal muscle weakness. 12428213 2002