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Congenital Hypothyroidism

Prevalence: 1/3000

endocrine

Official·OMIM:275200 Official·ORPHA442

Thyroid function disorder due to TSHR, TG, or other gene mutations.

Associated Genes

TSHRThyroid Stimulating Hormone Receptor

Chromosome 14Autosomal Recessive

TGThyroglobulin

Chromosome 8Autosomal Recessive