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602079
TMAU
TRIMETHYLAMINURIA
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Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Noonan Syndrome
Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Prader-Willi Syndrome
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Noonan Syndrome
Heart Diseases
Heart Defects, Congenital
Noonan Syndrome
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Hemorrhagic Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Prader-Willi Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Noonan Syndrome
Chromosome Disorders
Prader-Willi Syndrome
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Noonan Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Prader-Willi Syndrome
Metabolism, Inborn Errors
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Noonan Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Nutrition Disorders
Overnutrition
Obesity
Prader-Willi Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Signs and Symptoms
Signs and Symptoms, Digestive
Halitosis
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