Hypothyroidism, Congenital, Nongoitrous, 4 (*)

Alternative Names

  • CHNG4
  • Thyrotropin Deficiency, Isolated
  • Throid-Stimulating Hormone Deficiency
  • TSH Deficiency
  • Pituitary Cretinism
  • Thyrotropin, Biologically Inactive
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WHO-ICD-10 version:2010

Endocrine, nutritional and metabolic diseases

Disorders of thyroid gland

OMIM Number

275100

Mode of Inheritance

Autosomal recessive

Gene Map Locus

1p13.2

Epidemiology in the Arab World

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