familial periodic paralysis
Information
- Disease name
- familial periodic paralysis
- Disease ID
- DOID:1029
- Description
- "A metal metabolism disorder that is characterized by episodes of muscle paralysis in which the affected muscles become flaccid and the deep tendon reflexes disappear. Between the episodes the affected muscles usually work normally, and that are caused by mutations in genes involved in the sodium and calcium channels in nerve cells." [url:https\://www.cedars-sinai.org/health-library/diseases-and-conditions/p/periodic-paralysis.html, url:https\://www.ninds.nih.gov/Disorders/All-Disorders/Familial-Periodic-Paralyses-Information-Page]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:896
- Cross Reference ID (Disease Ontology)
- GARD:6422
- Cross Reference ID (Disease Ontology)
- ICD10CM:G72.3
- Cross Reference ID (Disease Ontology)
- MESH:D010245
- Cross Reference ID (Disease Ontology)
- NCI:C84709
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:193241004
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0030443