Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1771479014 | Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 1782578011 | Aplasia cutis congenita secondary to malformation syndrome (Type 9) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | morphologie associée (attribut) | Aplasia | true | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | est un(e) (attribut) | aplasia cutis congenita (trouble) | true | Inferred relationship | Some | ||
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | localisation d'une constatation (attribut) | Structure of skin region | false | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | morphologie associée (attribut) | Congenital absence | false | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | associé à (attribut) | Congenital malformation syndrome (disorder) | true | Inferred relationship | Some | 2 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | morphologie associée (attribut) | Congenital absence | false | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 2 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 2 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | morphologie associée (attribut) | Congenital partial absence | false | Inferred relationship | Some | 2 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | morphologie associée (attribut) | Congenital absence | false | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | localisation d'une constatation (attribut) | Skin part | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Oculocerebrocutaneous syndrome (disorder) | est un(e) (attribut) | True | Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Inferred relationship | Some |
Reference Sets
FHIR