Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3324723015 | Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3324724014 | Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3324725010 | Hyperinsulinism due to HNF1A deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency | Is a | Hyperinsulinism | true | Inferred relationship | Existential restriction modifier | ||
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency | Is a | Digestive system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Existential restriction modifier | ||
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency | Finding site | Endocrine pancreatic structure | false | Inferred relationship | Existential restriction modifier | ||
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency | Finding site | Endocrine pancreatic structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Hyperinsulinism due to hepatocyte nuclear factor 1-alpha deficiency | Is a | Congenital disease | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets