Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3315827019 | Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3315828012 | Primary ciliary dyskinesia and retinitis pigmentosa syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3315829016 | An X-linked ciliary dysfunction disorder of both the respiratory epithelium and photoreceptors of the retina. This leads to ocular problems including mild night blindness, constriction of the visual field and scotopic and photopic ERG responses reduced to 30-60%. It is also associated with primary ciliary dyskinesia manifestations including chronic bronchorrhea with bronchoectasis and chronic sinusitis along with sensorineural hearing loss. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3315830014 | An X-linked ciliary dysfunction disorder of both the respiratory epithelium and photoreceptors of the retina. This leads to ocular problems including mild night blindness, constriction of the visual field and scotopic and photopic ERG responses reduced to 30-60%. It is also associated with primary ciliary dyskinesia manifestations including chronic bronchorrhoea with bronchoectasis and chronic sinusitis along with sensorineural hearing loss. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
930151000172113 | syndrome de dyskinésie ciliaire primitive-rétinite pigmentaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
1756621000172119 | syndrome de dyskinésie ciliaire primitive avec rétinite pigmentaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
1014231000172116 | primaire ciliaire dyskinesie, retinitis pigmentosa-syndroom | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Is a | Retinitis pigmentosa | false | Inferred relationship | Some | ||
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Is a | Immotile cilia syndrome | false | Inferred relationship | Some | ||
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Is a | X-linked hereditary disease | false | Inferred relationship | Some | ||
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 3 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Finding site | Retinal structure | true | Inferred relationship | Some | 3 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 2 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Finding site | Retinal structure | false | Inferred relationship | Some | 2 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 3 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Associated morphology | defect | false | Inferred relationship | Some | 1 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Finding site | Respiratory tract structure | false | Inferred relationship | Some | 1 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Has interpretation | Impaired | true | Inferred relationship | Some | 4 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Interprets | Mucociliary clearance | true | Inferred relationship | Some | 4 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Is a | Inherited mucociliary clearance defect | true | Inferred relationship | Some | ||
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Is a | Developmental disorder | false | Inferred relationship | Some | ||
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Some | ||
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Is a | X-linked retinitis pigmentosa | true | Inferred relationship | Some | ||
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Finding site | Respiratory tract structure | true | Inferred relationship | Some | 2 | |
Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder) | Associated morphology | defect | false | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets