Paralyses, Familial Periodic
Disease ID: disease_node_5880
Connections displayed (default: 10).
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| Dbxref | GARD:6422, ICD10CM:G72.3, MESH:D010245, NCI:C84709, SNOMEDCT_US_2023_03_01:193241004, UMLS_CUI:C0030443 |
|---|---|
| Subclassof | DOID_896 |
| Data Source | DOID, MESH |
| Mesh Id | D010245 |
| Mesh Label | Paralyses, Familial Periodic |
| Mesh Subclassof | D008664, D009135 |
| Doid Label | familial periodic paralysis |
| Doid 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. |
| Disease Node Id | disease_node_5880 |
| Doid Id | DOID_1029 |
| Label | Paralyses, Familial Periodic |
- Outgoing r'ship
SUBCLASS_OFto/from Metal Metabolism, Inborn Errors(ID:disease_node_5173) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Paralysis, Hyperkalemic Periodic(ID:disease_node_10607) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Hypokalemic Periodic Paralysis(ID:disease_node_10611) (Disease)