Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3728164018 | Periodic paralysis with later-onset distal motor neuropathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3728165017 | Periodic paralysis with later-onset distal motor neuropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 7700781000146113 | periodieke paralyse met later optredende distale motorische neuropathie (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 7700791000146110 | periodieke paralyse met later optredende distale motorische neuropathie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3728166016 | A rare genetic neuromuscular disease with characteristics of acute episodic muscle weakness in upper and lower extremities (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Periodic paralysis with later-onset distal motor neuropathy (disorder) | Finding site | Peripheral nervous system structure | true | Inferred relationship | Some | 3 | |
| Periodic paralysis with later-onset distal motor neuropathy (disorder) | Interprets | Gross movement of body and limbs | true | Inferred relationship | Some | 1 | |
| Periodic paralysis with later-onset distal motor neuropathy (disorder) | Is a | Mitochondrial myopathy | true | Inferred relationship | Some | ||
| Periodic paralysis with later-onset distal motor neuropathy (disorder) | Is a | Myoneural disorder | true | Inferred relationship | Some | ||
| Periodic paralysis with later-onset distal motor neuropathy (disorder) | Has interpretation | Absent | true | Inferred relationship | Some | 1 | |
| Periodic paralysis with later-onset distal motor neuropathy (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 2 | |
| Periodic paralysis with later-onset distal motor neuropathy (disorder) | Is a | Periodic paralysis | true | Inferred relationship | Some | ||
| Periodic paralysis with later-onset distal motor neuropathy (disorder) | Interprets | Movement | true | Inferred relationship | Some | 4 | |
| Periodic paralysis with later-onset distal motor neuropathy (disorder) | Is a | Movement disorder | true | Inferred relationship | Some | ||
| Periodic paralysis with later-onset distal motor neuropathy (disorder) | Is a | Gross movement of body and limbs - finding | true | Inferred relationship | Some | ||
| Periodic paralysis with later-onset distal motor neuropathy (disorder) | Is a | Loss of motor function | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR