loading...| Preferred Name |
Hyperkalemic periodic paralysis |
| ID |
http://www.orpha.net/ORDO/Orphanet_682 |
| alternative_term |
HyperKPP Primary hyperPP Hyperkalemic PP Familial hyperPP HyperPP Familial hyperkalemic periodic paralysis HYPP Gamstorp disease Primary hyperkalemic periodic paralysis Gamstorp episodic adynamy Adynamia episodica hereditaria |
| definition |
A rare muscle disorder characterized by episodic attacks of muscle weakness associated with an increase in serum potassium concentration. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=682 |
| has_age_of_onset |
Childhood |
| has_inheritance |
Autosomal dominant |
| hasDbXref |
MeSH:C535409 OMIM:170500 UMLS:C0238357 MeSH:D020513 ICD-10:G72.3 ICD-11:8C74.11 |
| label |
Hyperkalemic periodic paralysis |
| notation |
ORPHA:682 |
| part_of |
http://www.orpha.net/ORDO/Orphanet_371433 |
| prefixIRI |
ORDO:Orphanet_682 |
| prefLabel |
Hyperkalemic periodic paralysis |
| present_in |
Netherlands AND has_point_prevalence_average_value : 0.06 AND has_point_prevalence_range : <1 / 1 000 000 Europe AND has_point_prevalence_average_value : 0.5 AND has_point_prevalence_range : 1-9 / 1 000 000 United Kingdom AND has_point_prevalence_average_value : 0.17 AND has_point_prevalence_range : 1-9 / 1 000 000 |
| treeView |
http://www.orpha.net/ORDO/Orphanet_371433 |
| subClassOf |