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GTR Home > Conditions/Phenotypes > Thyrotoxic periodic paralysis, susceptibility to, 2

Thyrotoxic periodic paralysis, susceptibility to, 2

Synonyms
Thyrotoxic periodic paralysis 2

Summary

Any thyrotoxic periodic paralysis in which the cause of the disease is a mutation in the KCNJ18 gene. [from MONDO]

Available tests

8 tests are in the database for this condition.

Clinical tests (8 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: KIR2.6, TTPP2, KCNJ18
    Summary: potassium inwardly rectifying channel subfamily J member 18

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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