loading...| Preferred Name |
Hypokalemic periodic paralysis |
| ID |
http://www.orpha.net/ORDO/Orphanet_681 |
| alternative_term |
Westphall disease |
| definition |
A rare genetic, muscle channelopathy characterized by recurrent episodic attacks of generalized muscle weakness associated with a decrease in blood potassium levels. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=681 |
| has_age_of_onset |
Adolescent Childhood |
| has_inheritance |
Autosomal dominant |
| hasDbXref |
MeSH:D020514 ICD-11:8C74.10 OMIM:170400 ICD-10:G72.3 UMLS:C0238358 OMIM:613345 |
| label |
Hypokalemic periodic paralysis |
| notation |
ORPHA:681 |
| part_of |
http://www.orpha.net/ORDO/Orphanet_98741 http://www.orpha.net/ORDO/Orphanet_98744 http://www.orpha.net/ORDO/Orphanet_371433 http://www.orpha.net/ORDO/Orphanet_98738 |
| prefixIRI |
ORDO:Orphanet_681 |
| prefLabel |
Hypokalemic periodic paralysis |
| present_in |
Europe AND has_point_prevalence_average_value : 1.0 AND has_point_prevalence_range : 1-9 / 100 000 Netherlands AND has_point_prevalence_average_value : 0.53 AND has_point_prevalence_range : 1-9 / 1 000 000 United Kingdom AND has_point_prevalence_average_value : 0.13 AND has_point_prevalence_range : 1-9 / 1 000 000 |
| treeView |
http://www.orpha.net/ORDO/Orphanet_98741 http://www.orpha.net/ORDO/Orphanet_98744 http://www.orpha.net/ORDO/Orphanet_371433 http://www.orpha.net/ORDO/Orphanet_98738 |
| subClassOf |