Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4667738012 | Hereditary growth hormone deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4667739016 | Hereditary growth hormone deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5343011000052117 | ärftlig brist på tillväxthormon | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary growth hormone deficiency (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
| Hereditary growth hormone deficiency (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Hereditary growth hormone deficiency (disorder) | Is a | Growth hormone deficiency (disorder) | true | Inferred relationship | Some | ||
| Hereditary growth hormone deficiency (disorder) | Finding site | Structure of pars distalis of pituitary (body structure) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Growth delay due to insulin-like growth factor type 1 deficiency (disorder) | Is a | True | Hereditary growth hormone deficiency (disorder) | Inferred relationship | Some | |
| Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome (disorder) | Is a | True | Hereditary growth hormone deficiency (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR