Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3308600014 | Hyperprolinemia type 2 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3308601013 | Hyperprolinemia type 2 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3308602018 | Hyperprolinaemia type 2 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3308603011 | Hyperprolinemia type II | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3308604017 | Hyperprolinaemia type II | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hyperprolinemia type 2 | Due to | Deficiency of pyrroline-5-carboxylate reductase | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hyperprolinemia type 2 | Is a | Hyperprolinemia | true | Inferred relationship | Existential restriction modifier | ||
| Hyperprolinemia type 2 | 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