Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 437707011 | Maternal phenylketonuria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 600471000241114 | phénylcétonurie maternelle (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 692533018 | Maternal phenylketonuria (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 929371000172114 | embryopathie hyperphénylalaninémique | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 939721000172114 | phénylcétonurie maternelle | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Maternal phenylketonuria | est un(e) (attribut) | Disorder of phenylalanine metabolism | true | Inferred relationship | Some | ||
| Maternal phenylketonuria | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Maternal phenylketonuria | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR