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Biological and Environmental Research Ontology
Last uploaded:
December 23, 2022
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| Id | http://purl.obolibrary.org/obo/NCIT_C84775
http://purl.obolibrary.org/obo/NCIT_C84775
|
|---|---|
| Preferred Name | Hypokalemic Periodic Paralysis |
| Definitions |
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.
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| 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
|
| prefLabel |
Hypokalemic Periodic Paralysis
|
| Preferred_Name |
Hypokalemic Periodic Paralysis
|
| UMLS_CUI |
C0238358
|
| prefixIRI |
NCIT:C84775
|
| subClassOf | |
| code |
C84775
|
| type | |
| Semantic_Type |
Disease or Syndrome
|
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