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 | Reference Sets |
| 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 | GB English: Preferred (foundation metadata concept) |
| 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 | GB English: Preferred (foundation metadata concept) |
| 2048801000052118 | aplasia cutis congenita sekundärt till missbildningssyndrom (typ 9) | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) | Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Is a | Aplasia cutis congenita | true | Inferred relationship | Some | ||
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Finding site | Structure of skin region | false | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Associated morphology | Congenital absence (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Associated with | Congenital malformation syndrome (disorder) | true | Inferred relationship | Some | 2 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Associated morphology | Congenital absence (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Associated morphology | medfödd partiell avsaknad | false | Inferred relationship | Some | 2 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Associated morphology | Congenital absence (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
| Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Finding site | Skin part | true | Inferred relationship | Some | 1 | |
| 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) | Associated morphology | Aplasia | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Oculo-cerebro-cutaneous syndrome (aplasia cutis, skin tags, eye & brain defects) (disorder) | Is a | True | Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR