loading...| Preferred Name | familial periodic paralysis | |
| Synonyms |
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| Definitions |
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. |
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| ID |
http://purl.obolibrary.org/obo/DOID_1029 |
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| database_cross_reference |
ICD10CM:G72.3 MESH:D010245 SNOMEDCT_US_2023_03_01:193241004 UMLS_CUI:C0030443 GARD:6422 NCI:C84709 |
|
| definition |
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. |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:1029 |
|
| in_subset | ||
| label |
familial periodic paralysis |
|
| notation |
DOID:1029 |
|
| note |
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. |
|
| preferred label |
familial periodic paralysis |
|
| prefLabel |
familial periodic paralysis |
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| subClassOf |