Hypothyroidism due to TSH receptor mutations

Definition

A type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth due to thyroid resistance to TSH.

Disease data

Classification

Disease

ORPHA code

90673

OMIM code

275200

ICD10 code

E03.1

ICD11 code

*Soruce

No additional description.

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Description of the disease *