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Query OMIM entry list
605356
YWHAG
TYROSINE 3-MONOOXYGENASE/TRYPTOPHAN 5-MONOOXYGENASE ACTIVATION PROTEIN, GAMMA ISOFORM
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Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Williams Syndrome
Cardiovascular Diseases
Heart Diseases
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Supravalvular
Williams Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Williams Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Williams Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
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