| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/613239 |
| Similar Terms | |
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1 genes associated with the {thyrotoxic periodic paralysis, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| KCNJ18 | potassium channel, inwardly rectifying subfamily J, member 18 |