Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
69704017 | Neurological muscle weakness | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
69705016 | Neurological muscle paresis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
778613011 | Neurological muscle weakness (finding) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3084441000005119 | neurologisk betinget kraftnedsættelse | da | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Danish module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Neurological muscle weakness | Is a | Muscle weakness | true | Inferred relationship | Some | ||
Neurological muscle weakness | Finding site | Structure of nervous system (body structure) | false | Inferred relationship | Some | ||
Neurological muscle weakness | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Neurological muscle weakness | Interprets | Nervous system function | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
A clinically heterogeneous progressive condition with characteristics of a combination of proximal neurogenic muscle weakness, sensory-motor neuropathy, ataxia, and pigmentary retinopathy. NARP syndrome is a maternally inherited syndrome and women can transmit to all their offspring. Clinical severity usually depends on the mutation load. | Is a | True | Neurological muscle weakness | Inferred relationship | Some |
This concept is not in any reference sets