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Query OMIM entry list
607200
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THYROID HORMONOGENESIS, GENETIC DEFECT IN, 6
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Congenital Hypothyroidism
Bone Diseases, Endocrine
Congenital Hypothyroidism
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Thyroid Dysgenesis
Genetic Diseases, Inborn
Dwarfism
Congenital Hypothyroidism
Endocrine System Diseases
Dwarfism
Congenital Hypothyroidism
Thyroid Diseases
Hypothyroidism
Congenital Hypothyroidism
Thyroid Dysgenesis
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