Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3331427010 | Agnathia, holoprosencephaly, situs inversus syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3331429013 | Agnathia, holoprosencephaly, situs inversus syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3331430015 | An extremely rare and fatal association syndrome with characteristics of absence of the mandible, cerebral malformations with facial anomalies related to a defect in cleavage in the embryonic brain (e.g. synophthalmia, malformed and low-set ears fused in midline, agenesis of the olfactory bulbs, microstomia, hypoglossia/aglossia) and situs inversus partialis or totalis. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Agnathia, holoprosencephaly, situs inversus syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Agnathia, holoprosencephaly, situs inversus syndrome | Finding site | Bone structure of mandible | true | Inferred relationship | Some | 1 | |
Agnathia, holoprosencephaly, situs inversus syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Agnathia, holoprosencephaly, situs inversus syndrome | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Agnathia, holoprosencephaly, situs inversus syndrome | Associated morphology | Morphologically abnormal structure | false | Inferred relationship | Some | 2 | |
Agnathia, holoprosencephaly, situs inversus syndrome | Finding site | Face structure | false | Inferred relationship | Some | 2 | |
Agnathia, holoprosencephaly, situs inversus syndrome | Pathological process | Pathological developmental process | false | Inferred relationship | Some | 2 | |
Agnathia, holoprosencephaly, situs inversus syndrome | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Agnathia, holoprosencephaly, situs inversus syndrome | Is a | Holoprosencephaly sequence | true | Inferred relationship | Some | ||
Agnathia, holoprosencephaly, situs inversus syndrome | Is a | Congenital micrognathism | true | Inferred relationship | Some | ||
Agnathia, holoprosencephaly, situs inversus syndrome | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Agnathia, holoprosencephaly, situs inversus syndrome | Is a | Inherited disorder of connective tissue | false | Inferred relationship | Some | ||
Agnathia, holoprosencephaly, situs inversus syndrome | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Agnathia, holoprosencephaly, situs inversus syndrome | Associated morphology | Hypoplasia | false | Inferred relationship | Some | 2 | |
Agnathia, holoprosencephaly, situs inversus syndrome | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Agnathia, holoprosencephaly, situs inversus syndrome | Finding site | Bone structure of mandible | false | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set