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hypothyroidism, congenital, nongoitrous, 5 | RareConnect | RareConnect.io

/hypothyroidism, congenital, nongoitrous

/hypothyroidism, congenital, nongoitrous, 5

hypothyroidism, congenital, nongoitrous, 5

Rare Disease

MONDO:0009154

Also Known As

CHNG5NKX2-5 hypothyroidism, congenital, nongoitroushypothyroidism, congenital nongoitrous, 5hypothyroidism, congenital, nongoitrous caused by mutation in NKX2-5hypothyroidism, congenital, nongoitrous, 5hypothyroidism, congenital, nongoitrous, type 5congenital nongoitrous hypothyroidism 5

Definition

Any hypothyroidism, congenital, nongoitrous in which the cause of the disease is a mutation in the NKX2-5 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

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

External Resources

OMIM

OMIM:225250 ↗

GARD

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