MYL2, myosin light chain 2, 4633

N. diseases: 104; N. variants: 28
Disease: Obstructive asymmetric septal hypertrophy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0597124
Disease: Obstructive asymmetric septal hypertrophy
Obstructive asymmetric septal hypertrophy 		0.300 Biomarker disease CTD_human Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy. 9241277 1997