Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2023. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5234014015 | Sodium voltage-gated channel alpha subunit 9-related congenital insensitivity to pain | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5234015019 | Congenital insensitivity to pain, anosmia, neuropathic arthropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5234016018 | SCN9A-related congenital insensitivity to pain | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5234017010 | Congenital insensitivity to pain, anosmia, neuropathic arthropathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5400702012 | A rare genetic peripheral neuropathy characterized by complete congenital insensitivity to painful stimuli, commonly associated with neuropathic arthropathy. In addition, patients are typically anosmic. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400703019 | A rare genetic peripheral neuropathy characterised by complete congenital insensitivity to painful stimuli, commonly associated with neuropathic arthropathy. In addition, patients are typically anosmic. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5234014015 | Sodium voltage-gated channel alpha subunit 9-related congenital insensitivity to pain | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5234015019 | Congenital insensitivity to pain, anosmia, neuropathic arthropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5234016018 | SCN9A-related congenital insensitivity to pain | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5234017010 | Congenital insensitivity to pain, anosmia, neuropathic arthropathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5234018017 | A rare genetic peripheral neuropathy with characteristics of complete congenital insensitivity to painful stimuli commonly associated with neuropathic arthropathy. In addition, patients are typically anosmic. Caused by homozygous or compound heterozygous mutations in the SCN9A gene on chromosome 2q24. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400702012 | A rare genetic peripheral neuropathy characterized by complete congenital insensitivity to painful stimuli, commonly associated with neuropathic arthropathy. In addition, patients are typically anosmic. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5400703019 | A rare genetic peripheral neuropathy characterised by complete congenital insensitivity to painful stimuli, commonly associated with neuropathic arthropathy. In addition, patients are typically anosmic. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)