Human Phenotype Ontology 
Grandparent Node:
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Paralysis (HP:0003470)help
Parent Node:
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Periodic paralysis (HP:0003768)help
..Starting node
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Periodic hyperkalemic paralysis (HP:0007215)help
Term ID: 7215
Name: Periodic hyperkalemic paralysis
Synonym: Hyperkalemic periodic paralysis
Definition: Episodes of muscle weakness associated with elevated levels of potassium in the blood.
Comments:
Reference: HP:0007215
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPeriodic hypokalemic paresis (HP:0008153) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007215HP:0007215Periodic hyperkalemic paralysis0KCNJ2 CL E G H37596263ORPHA:37553Andersen-Tawil syndromeHP:0040283 - Occasional193
HP:0007215HP:0007215Periodic hyperkalemic paralysis0KCNJ5 CL E G H37626266ORPHA:37553Andersen-Tawil syndromeHP:0040283 - Occasional128
HP:0007215HP:0007215Periodic hyperkalemic paralysis0SCN4A CL E G H632910591ORPHA:682Hyperkalemic periodic paralysisHP:0040281 - Very frequent263
HP:0007215HP:0007215Periodic hyperkalemic paralysis0SCN4A CL E G H632910591OMIM:170500Hyperkalemic periodic paralysis.263


Genes (3) :KCNJ2 KCNJ5 SCN4A

Diseases (3) :ORPHA:37553 ORPHA:682 OMIM:170500
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.