Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 50489017 | Childhood hypophosphatasia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 50490014 | Hypophosphatasia, childhood type | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 50491013 | Juvenile hypophosphatasia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 761149017 | Childhood hypophosphatasia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Childhood hypophosphatasia | Is a | Hypophosphatasia | true | Inferred relationship | Existential restriction modifier | ||
| Childhood hypophosphatasia | Is a | Autosomal hereditary disorder | false | Inferred relationship | Existential restriction modifier | ||
| Childhood hypophosphatasia | Is a | Enzymopathy | true | Inferred relationship | Existential restriction modifier | ||
| Childhood hypophosphatasia | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 | |
| Childhood hypophosphatasia | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Childhood hypophosphatasia | Occurrence | Childhood | true | Inferred relationship | Existential restriction modifier | 1 | |
| Childhood hypophosphatasia | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR