Congenital nongoitrous hypothyroidism 3

MONDO:0012360

A congenital hypothyroidism characterized by autosomal dominant inheritance of resistance to thyrotropin that has material basis in variation in the chromosome region 15q25.3-q26.1.

Also known as: CHNG3, hypothyroidism, congenital, nongoitrous, 3, resistance to thyrotropin, thyrotropin resistance

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Broader categories

Disease (680) Hereditary disease (176) Thyroid gland disorder (89) Endocrine system disorder (72) Hypothyroidism (42) Hereditary endocrine growth disease (24) Human disease (14) Congenital hypothyroidism (10) Disease of genetic or genomic mechanism (2) Permanent congenital hypothyroidism (1)

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