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Query OMIM entry list
274800
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THYROID HORMONOGENESIS, GENETIC DEFECT IN, 4
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Endocrine System Diseases
Thyroid Diseases
Goiter
Hypothyroidism
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
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