Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3498731014 | Isolated hereditary congenital facial paralysis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3498732019 | Isolated hereditary congenital facial paralysis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3499970018 | An extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or asymmetrical facial palsy. Involvement of the branches of the facial nerve can be unequal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Isolated hereditary congenital facial paralysis (disorder) | Is a | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
Isolated hereditary congenital facial paralysis (disorder) | Is a | Congenital anomaly of peripheral nerve | true | Inferred relationship | Some | ||
Isolated hereditary congenital facial paralysis (disorder) | Is a | Congenital facial nerve palsy (disorder) | true | Inferred relationship | Some | ||
Isolated hereditary congenital facial paralysis (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Isolated hereditary congenital facial paralysis (disorder) | Has interpretation | Absent | true | Inferred relationship | Some | 2 | |
Isolated hereditary congenital facial paralysis (disorder) | Interprets | Gross movement of body and limbs | false | Inferred relationship | Some | 2 | |
Isolated hereditary congenital facial paralysis (disorder) | Associated morphology | Aplasia | false | Inferred relationship | Some | 3 | |
Isolated hereditary congenital facial paralysis (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Isolated hereditary congenital facial paralysis (disorder) | Finding site | Facial nerve structure | false | Inferred relationship | Some | 3 | |
Isolated hereditary congenital facial paralysis (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Isolated hereditary congenital facial paralysis (disorder) | Associated morphology | Aplasia | true | Inferred relationship | Some | 1 | |
Isolated hereditary congenital facial paralysis (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Isolated hereditary congenital facial paralysis (disorder) | Finding site | Facial nerve structure | true | Inferred relationship | Some | 1 | |
Isolated hereditary congenital facial paralysis (disorder) | Is a | Congenital anomaly of nervous system of head/neck (disorder) | true | Inferred relationship | Some | ||
Isolated hereditary congenital facial paralysis (disorder) | Interprets | Movement | true | Inferred relationship | Some | 3 | |
Isolated hereditary congenital facial paralysis (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Isolated hereditary congenital facial paralysis (disorder) | Interprets | Movement observable | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets