Congenital nongoitrous hypothyroidism 6

MONDO:0013757

Any hypothyroidism, congenital, nongoitrous in which the cause of the disease is a mutation in the THRA gene.

Also known as: CHNG6, THRA hypothyroidism, congenital, nongoitrous, hypothyroidism, congenital, nongoitrous caused by mutation in THRA, hypothyroidism, congenital, nongoitrous, 6, hypothyroidism, congenital, nongoitrous, type 6

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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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