Status: current, Primitive. Date: 31-Oct 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4643796019 | Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
4643797011 | Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4643798018 | A rare syndromic frontonasal dysplasia with characteristics of distinctive facial dysmorphic features including hypertelorism, almond-shaped palpebral fissures, nasal deformity with creased ridge, depressed or absent tip and asymmetry and partial absence of nasal bones and downturned corners of the mouth. Additional reported manifestations are limb anomalies (e. g. Poland anomaly, transverse limb agenesis and anomalies of the hands and feet such as camptodactyly, oligodactyly, clinodactyly and syndactyly), frontonasal encephalocele, choanal atresia, congenital renal/cardiac malformations, and corpus callosum agenesis. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome | Is a | Genetic disease | true | Inferred relationship | Some | ||
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome | Is a | Frontonasal dysplasia sequence | true | Inferred relationship | Some | ||
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome | Finding site | Bone structure of cranium | true | Inferred relationship | Some | 1 | |
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome | Finding site | Face structure | true | Inferred relationship | Some | 2 | |
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Some | 2 | |
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set