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Thyrotoxic periodic paralysis, susceptibility to, 2

MONDO:0013193

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

Also known as: KCNJ18 thyrotoxic periodic paralysis, thyrotoxic periodic paralysis caused by mutation in KCNJ18, thyrotoxic periodic paralysis, susceptibility to, 2, thyrotoxic periodic paralysis, susceptibility to, type 2, TTPP2

0 clinical trials for this condition and its sub-types, 0 tagged with Thyrotoxic periodic paralysis, susceptibility to, 2 itself.

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Including sub-types (0) Tagged with Thyrotoxic periodic paralysis, susceptibility to, 2 (0)

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