Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
101151019 | Hormone secretion | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
1203960014 | Hormone secretion, function (observable entity) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
2671865011 | Hormone secretion, function | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hormone secretion, function | Is a | Endocrine function | true | Inferred relationship | Existential restriction modifier | ||
Hormone secretion, function | Inheres in | Structure of endocrine system | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Hypoparathyroidism due to Wilson disease | Interprets | True | Hormone secretion, function | Inferred relationship | Existential restriction modifier | 1 |
Sanjad Sakati syndrome | Interprets | True | Hormone secretion, function | Inferred relationship | Existential restriction modifier | 3 |
Sagliker syndrome | Interprets | True | Hormone secretion, function | Inferred relationship | Existential restriction modifier | 3 |
Autosomal dominant familial isolated hypoparathyroidism | Interprets | True | Hormone secretion, function | Inferred relationship | Existential restriction modifier | 1 |
Autosomal recessive familial isolated hypoparathyroidism | Interprets | True | Hormone secretion, function | Inferred relationship | Existential restriction modifier | 1 |
46,XX ovarian dysgenesis, short stature syndrome | Interprets | True | Hormone secretion, function | Inferred relationship | Existential restriction modifier | 2 |
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This concept is not in any reference sets