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GTR Home > Conditions/Phenotypes > Hypothyroidism, congenital, nongoitrous, 5

Hypothyroidism, congenital, nongoitrous, 5

Summary

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

Available tests

48 tests are in the database for this condition.

Clinical tests (48 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CHNG5, CSX, CSX1, HLHS2, NKX2.5, NKX2E, NKX4-1, VSD3, NKX2-5
    Summary: NK2 homeobox 5

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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