Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3758240013 | A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3758241012 | A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalised areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3758242017 | Acute pure sensory Guillain-Barré syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3758243010 | Acute pure sensory neuropathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3758244016 | Acute pure sensory neuropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. | Is a | Guillain-Barré syndrome | true | Inferred relationship | Some | ||
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. | Associated morphology | Demyelination | true | Inferred relationship | Some | 2 | |
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. | Clinical course | Sudden onset AND/OR short duration (qualifier value) | true | Inferred relationship | Some | 3 | |
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 2 | |
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. | Finding site | Nerve structure | false | Inferred relationship | Some | 1 | |
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. | Associated morphology | Inflammation | false | Inferred relationship | Some | 1 | |
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Some | 1 | |
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Some | 2 | |
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 1 | |
A acquired demyelinating neuropathy disease with characteristics of acute symmetric monophasic sensory neuropathy without motor involvement, typically manifesting with numbness in the distal lower limbs which progressively extends to all the limb, tingling sensation in the distal lower limbs, generalized areflexia and unsteady gait as well as clumsiness of the upper limbs, pseudoathetosis and loss of vibration sense. | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets