Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3760281019 | Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3760282014 | Autosomal recessive hyperinsulinism due to SUR1 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3760283016 | Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3760284010 | Autosomal recessive hyperinsulinemic hypoglycemia due to SUR1 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3760285011 | Autosomal recessive hyperinsulinemic hypoglycaemia due to SUR1 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency | Is a | Digestive system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency | Is a | Hyperinsulinism | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency | Is a | Hereditary disorder of endocrine system | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 deficiency | Finding site | Endocrine pancreatic structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive hyperinsulinism due to sulfonylurea receptor 1 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
FHIR