Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3531629010 | Developmental anomaly of periodontal tissue | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3531630017 | Developmental anomaly of periodontal tissue (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
6075581000241115 | anomalie du développement du tissu parodontal | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6075591000241118 | anomalie développementale du tissu périodontal | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Developmental anomaly of periodontal tissue | Is a | Periodontal disease | true | Inferred relationship | Some | ||
Developmental anomaly of periodontal tissue | Associated morphology | anomalie du développement | false | Inferred relationship | Some | 1 | |
Developmental anomaly of periodontal tissue | Finding site | Periodontal tissues structure | true | Inferred relationship | Some | 1 | |
Developmental anomaly of periodontal tissue | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Developmental anomaly of periodontal tissue | Is a | Developmental disorder | true | Inferred relationship | Some | ||
Developmental anomaly of periodontal tissue | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Periodontal Ehlers-Danlos syndrome (disorder) | Is a | False | Developmental anomaly of periodontal tissue | Inferred relationship | Some | |
Radicular cyst | Is a | False | Developmental anomaly of periodontal tissue | Inferred relationship | Some | |
Hyperplastic tooth follicle | Is a | False | Developmental anomaly of periodontal tissue | Inferred relationship | Some | |
A rare genetic syndromic intellectual disability that is characterized by congenital permanent alopecia universalis, intellectual disability, psychomotor epilepsy and periodontitis (pyorrhea). Total permanent alopecia and pyorrhea are invariably concomitant while intellectual disability and psychomotor epilepsy are observed in most patients. No other abnormality of nails or skin (apart from absence of hair) has been reported. Transmission is autosomal dominant. | Is a | True | Developmental anomaly of periodontal tissue | Inferred relationship | Some |
This concept is not in any reference sets