Hypothyroidism, Congenital, Nongoitrous, 2 (CHNG2)

Hypothyroidism, Congenital, Nongoitrous, 2(来自ICD-11)

别称:

Thyroid Dysgenesis

Thyroid Hypoplasia

Thyroid Hemiagenesis

Chng2

Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia

Congenital Nongoitrous Hypothyroidism 2

Athyreotic Hypothyroidism

Thyrotropin Resistance

Thyroid Agenesis

Rtsh

Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia, Type 2

Congenital Hypothyroidism Due to Thyroid Dysgenesis or Hypoplasia

Hypothyroidism, Congenital, Due to Thyroid Dysgenesis

Congenital Hypothyroidism Due to Thyroid Dysgenesis

Hypothyroidism, Congenital, Non-Goitrous, 2

Hypothyroidism, Congenital, Nongoitrous, 1

Hypothyroidism, Congenital, Nongoitrous, 3

Thyroid-Stimulating Hormone Resistance

Thyroid Hormone Resistance Syndrome

Hypothyroidism, Athyreotic

Resistance to Thyrotropin

Thyroid, Ectopic

Thyroid Ectopic

Ectopic Thyroid

Thyrotropin

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Hypothyroidism, Congenital, Nongoitrous, 2, also known as thyroid dysgenesis, is related to bamforth-lazarus syndrome and athyreosis. An important gene associated with Hypothyroidism, Congenital, Nongoitrous, 2 is PAX8 (Paired Box 8), and among its related pathways/superpathways is Thyroxine (thyroid hormone) production. The drugs Dexamethasone and Dexamethasone acetate have been mentioned in the context of this disorder. Affiliated tissues include thyroid and pituitary, and related phenotypes are constipation and hypothyroidism

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