MeSH Treeview
Query OMIM entry list
160720
MYH3
MYOSIN, HEAVY CHAIN 3, SKELETAL MUSCLE, EMBRYONIC
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Musculoskeletal Diseases
Joint Diseases
Arthrogryposis
Muscular Diseases
Arthrogryposis
Musculoskeletal Abnormalities
Arthrogryposis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Musculoskeletal Abnormalities
Arthrogryposis
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Database Center for Life Science
