Hypothyroidism due to deficient transcription factors involved in pituitary development or function

Orpha code: 226307OMIM code:

Definition

Hypothyroidism due to mutations in transcription factors involved in pituitary development or function is a type of central congenital hypothyroidism (see this term), a permanent thyroid deficiency that is present from birth, characterized by low levels of thyroid hormones caused by disorders in the development or function of the pituitary.

Disease data
Classification

Disease

ORPHA code
226307
OMIM code
-
ICD10 code
E03.1
ICD11 code
5A00.01

No additional description.

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