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 (4)
DOID:14452 - hypokalemic periodic paralysis


Disease Ontology Definition:n_a

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

In OMIM:
OMIM:170400 - HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1; HOKPP1
OMIM:613345 - HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2; HOKPP2

In Mondo Disease Ontology:
MONDO:0008223 - hypokalemic periodic paralysis

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : scn4a, cacna1s, kcne3, atp1a2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): familial periodic paralysis (is_a)