| Preferred Name |
Hypokalemic Periodic Paralysis |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84775 |
| code |
C84775 |
| DEFINITION |
A rare, autosomal dominant inherited disorder characterized by irregular episodes of muscle weakness or paralysis which are always accompanied by low levels of potassium in the blood. |
| label |
Hypokalemic Periodic Paralysis |
| Preferred_Name |
Hypokalemic Periodic Paralysis |
| prefixIRI |
C84775 |
| prefLabel |
Hypokalemic Periodic Paralysis |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0238358 |
| subClassOf |