Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:14452 - hypokalemic periodic paralysis

Disease Ontology Definition:n_a

Synonyms: familial hypokalemic periodic paralysis, familial hypokalemic periodic paralysis (disorder), familial periodic paralysis, familial periodic paralysis (& [hypokalaemic]), Hypokalemic familial periodic paralysis, Hypokalemic periodic paralysis, Hypokalemic periodic paralysis (disorder), periodic hypokalemic paralysis, Periodic paralysis I, Westphal disease

Xenbase Genes : scn4a, cacna1s, kcne3, atp1a2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008223 - hypokalemic periodic paralysis


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): familial periodic paralysis (is_a)