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 |
| 50489017 | Childhood hypophosphatasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 50490014 | Hypophosphatasia, childhood type | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 50491013 | Juvenile hypophosphatasia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 761149017 | Childhood hypophosphatasia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Childhood hypophosphatasia | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Childhood hypophosphatasia | est un(e) (attribut) | Hypophosphatasia | true | Inferred relationship | Some | ||
| Childhood hypophosphatasia | est un(e) (attribut) | Autosomal hereditary disorder | false | Inferred relationship | Some | ||
| Childhood hypophosphatasia | est un(e) (attribut) | Enzymopathy | true | Inferred relationship | Some | ||
| Childhood hypophosphatasia | survenue (attribut) | congénital | true | Inferred relationship | Some | 2 | |
| Childhood hypophosphatasia | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Childhood hypophosphatasia | survenue (attribut) | enfance | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR