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FHIR
© HL7.org
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Server Home |
FHIR Server FHIR Server 3.7.4-SNAPSHOT
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FHIR Version n/a
User: [n/a]
Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3311172019 | Familial congenital hypopituitarism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3311175017 | Combined pituitary hormone deficiency genetic form (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3311409015 | Combined pituitary hormone deficiency genetic form | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3311410013 | Multiple pituitary hormone deficiency genetic form | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5401701013 | Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401702018 | Congenital hypopituitarism is characterised by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Combined pituitary hormone deficiency genetic form (disorder) | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
| Combined pituitary hormone deficiency genetic form (disorder) | Is a | Hypopituitarism | true | Inferred relationship | Some | ||
| Combined pituitary hormone deficiency genetic form (disorder) | Is a | Hereditary disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
| Combined pituitary hormone deficiency genetic form (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Combined pituitary hormone deficiency genetic form (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Combined pituitary hormone deficiency genetic form (disorder) | Finding site | Pituitary structure | false | Inferred relationship | Some | ||
| Combined pituitary hormone deficiency genetic form (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Combined pituitary hormone deficiency genetic form (disorder) | Finding site | Pituitary structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)