Familial thyroid dyshormonogenesis

Orpha code: 95716OMIM code: 607200

Definition

Familial thyroid dyshormonogenesis is a type of primary congenital hypothyroidism (see this term), a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis.

Disease data
Classification

Disease

Synonyms
Thyroid dyshormonogenesis
Rodzinna dyshormonogeneza tarczycy
ORPHA code
95716
OMIM code
607200
ICD10 code
E03.1
ICD11 code
-

No additional description.

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