Status: current, Defined. 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 | Case insensitive | SNOMED CT core |
| 4667739016 | Hereditary growth hormone deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary growth hormone deficiency | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Some | ||
| Hereditary growth hormone deficiency | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Hereditary growth hormone deficiency | Is a | Growth hormone deficiency | true | Inferred relationship | Some | ||
| Hereditary growth hormone deficiency | Finding site | Structure of distal part of pituitary | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Growth delay due to insulin-like growth factor type 1 deficiency | Is a | True | Hereditary growth hormone deficiency | Inferred relationship | Some | |
| Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome | Is a | True | Hereditary growth hormone deficiency | Inferred relationship | Some |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set