/congenital nongoitrous hypothyroidism 6

congenital nongoitrous hypothyroidism 6

Rare Disease

MONDO:0013757

Also Known As

CHNG6THRA hypothyroidism, congenital, nongoitrouscongenital nongoitrous hypothyroidism 6hypothyroidism, congenital, nongoitrous caused by mutation in THRAhypothyroidism, congenital, nongoitrous, 6hypothyroidism, congenital, nongoitrous, type 6

Definition

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

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Associated Genes

THRA ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:614450 ↗

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