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DO Term : familial periodic paralysis [DOID:1029] Disease Ontology

Namespace  disease_ontology Obsolete  false
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.
  • synonyms:
  • ICD10CM:G72.3,
  • NCI:C84709,
  • MESH:D010245,
  • UMLS_CUI:C0030443,
  • SNOMEDCT_US_2023_03_01:193241004,
  • GARD:6422
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents