Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4634887019 | SIX homeobox 2-related frontonasal dysplasia (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4634888012 | SIX2-related frontonasal dysplasia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4634889016 | SIX homeobox 2-related frontonasal dysplasia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5399366016 | A rare frontonasal dysplasia characterized by a craniofacial phenotype comprising frontal bossing with high anterior hairline, ptosis, hypertelorism, epicanthus inversus, flat nasal bridge, and broad nasal tip. Large anterior fontanelle, sagittal synostosis, and cranial base anomalies have also been described. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5399367013 | A rare frontonasal dysplasia characterised by a craniofacial phenotype comprising frontal bossing with high anterior hairline, ptosis, hypertelorism, epicanthus inversus, flat nasal bridge, and broad nasal tip. Large anterior fontanelle, sagittal synostosis, and cranial base anomalies have also been described. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
SIX homeobox 2-related frontonasal dysplasia (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
SIX homeobox 2-related frontonasal dysplasia (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
SIX homeobox 2-related frontonasal dysplasia (disorder) | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
SIX homeobox 2-related frontonasal dysplasia (disorder) | Is a | Frontonasal dysplasia sequence | true | Inferred relationship | Some | ||
SIX homeobox 2-related frontonasal dysplasia (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
SIX homeobox 2-related frontonasal dysplasia (disorder) | Finding site | Bone structure of cranium | true | Inferred relationship | Some | 1 | |
SIX homeobox 2-related frontonasal dysplasia (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
SIX homeobox 2-related frontonasal dysplasia (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
SIX homeobox 2-related frontonasal dysplasia (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
SIX homeobox 2-related frontonasal dysplasia (disorder) | Finding site | Face structure | true | Inferred relationship | Some | 2 | |
SIX homeobox 2-related frontonasal dysplasia (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
SIX homeobox 2-related frontonasal dysplasia (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)