Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3323444010 | Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3323445011 | Developmental delay, epilepsy, neonatal diabetes syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3323446012 | DEND syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3323447015 | DEND (developmental delay, epilepsy, neonatal diabetes) syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402595013 | DEND syndrome is a very rare, generally severe form of neonatal diabetes mellitus characterized by a triad of developmental delay, epilepsy, and neonatal diabetes. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402596014 | DEND syndrome is a very rare, generally severe form of neonatal diabetes mellitus characterised by a triad of developmental delay, epilepsy, and neonatal diabetes. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Is a | Neonatal diabetes mellitus | true | Inferred relationship | Some | ||
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Is a | Epilepsy | true | Inferred relationship | Some | ||
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Is a | Developmental delay | true | Inferred relationship | Some | ||
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Occurrence | Infancy | false | Inferred relationship | Some | 1 | |
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Finding site | Cerebrum | true | Inferred relationship | Some | 3 | |
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Finding site | Structure of endocrine system (body structure) | false | Inferred relationship | Some | 2 | |
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Has definitional manifestation | Seizure | false | Inferred relationship | Some | ||
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 4 | |
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Is a | Neonatal metabolic disorder (disorder) | true | Inferred relationship | Some | ||
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Is a | Neonatal disorder of endocrine system (disorder) | true | Inferred relationship | Some | ||
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Is a | Genetic disease | true | Inferred relationship | Some | ||
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Occurrence | Neonatal | true | Inferred relationship | Some | 1 | |
Developmental delay, epilepsy, neonatal diabetes syndrome (disorder) | Finding site | Structure of endocrine system (body 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)