MeSH Treeview
Query OMIM entry list
115210
RCM1
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1
→
High-scoring List
Musculoskeletal Diseases
Muscular Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Noonan Syndrome
Nervous System Diseases
Neuromuscular Diseases
Muscular Diseases
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Noonan Syndrome
Heart Diseases
Arrhythmias, Cardiac
Heart Block
Cardiac Output, Low
Cardiomegaly
Cardiomyopathies
Cardiomyopathy, Hypertrophic
Cardiomyopathy, Restrictive
Endomyocardial Fibrosis
Heart Defects, Congenital
Noonan Syndrome
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Subvalvular
Cardiomyopathy, Hypertrophic
Hemic and Lymphatic Diseases
Hematologic Diseases
Leukocyte Disorders
Eosinophilia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Cardiovascular Abnormalities
Heart Defects, Congenital
Noonan Syndrome
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Noonan Syndrome
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Noonan Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Proteostasis Deficiencies
Amyloidosis
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Cardiomegaly
Pathologic Processes
Arrhythmias, Cardiac
Heart Block
Fibrosis
Signs and Symptoms
Cardiac Output, Low
Database Center for Life Science