Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3725352019 | Hereditary infantile gigantism | en | Synonym | Active | Case insensitive | SNOMED CT core |
3725353012 | Familial infantile gigantism (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3725354018 | Familial infantile gigantism | en | Synonym | Active | Case insensitive | SNOMED CT core |
3725356016 | Infantile gigantism due to pituitary hyperplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
3725357013 | A rare genetic endocrine disease with characteristics of early-onset (before the age of five years old) excessive acceleration of linear growth and body size due to pituitary mixed growth hormone and prolactin secreting adenomas and/or mixed-cell pituitary hyperplasia. Patients present gigantism and may associate acromegalic features (for example coarse facial features, frontal bossing, prognathism, increased interdental space) as well as marked enlargement of hands and feet, soft tissue swelling, appetite increase and acanthosis nigricans. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
X-linked acrogigantism due to Xq26 microduplication | Is a | True | Familial infantile gigantism | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set