Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3701201017 | Congenital hypoplasia of entire upper limb (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3701202012 | Congenital hypoplasia of entire upper limb | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital hypoplasia of entire upper limb | Associated morphology | Hypoplasia | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital hypoplasia of entire upper limb | Finding site | Entire upper limb | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital hypoplasia of entire upper limb | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital hypoplasia of entire upper limb | Is a | Hypoplasia of upper limb | true | Inferred relationship | Existential restriction modifier | ||
| Congenital hypoplasia of entire upper limb | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR