Status: current, Defined. Date: 31-Jul 2004. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4546423014 | Family history of chromosomal anomaly (situation) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4546424015 | Family history of chromosomal anomaly | en | Synonym | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Family history of complete trisomy 21 syndrome | Is a | True | Family history of chromosomal anomaly | Inferred relationship | Some | |
Family history of Prader-Willi syndrome | Is a | False | Family history of chromosomal anomaly | Inferred relationship | Some | |
Family history of fragile X syndrome | Is a | True | Family history of chromosomal anomaly | Inferred relationship | Some | |
Family history of trisomy 13 | Is a | True | Family history of chromosomal anomaly | Inferred relationship | Some | |
Family history of trisomy 18 | Is a | True | Family history of chromosomal anomaly | Inferred relationship | Some | |
Family history of Turner syndrome | Is a | True | Family history of chromosomal anomaly | Inferred relationship | Some | |
Family history of sex chromosome aneuploidy | Is a | True | Family history of chromosomal anomaly | Inferred relationship | Some |
Reference Sets
Situation with explicit context foundation reference set
Problem/Diagnosis reference set