Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4535635012 | Congenital endocardial fibroelastosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4535636013 | Congenital endocardial fibroelastosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4535637016 | Fibroelastosis cordis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5857731000241116 | fibroélastose endocardique congénitale | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
5857741000241114 | élastomyofibrose congénitale | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital endocardial fibroelastosis (disorder) | Is a | Congenital heart disease | true | Inferred relationship | Some | ||
Congenital endocardial fibroelastosis (disorder) | Is a | Endocardial fibroelastosis | true | Inferred relationship | Some | ||
Congenital endocardial fibroelastosis (disorder) | Associated morphology | Fibroelastosis | true | Inferred relationship | Some | 1 | |
Congenital endocardial fibroelastosis (disorder) | Finding site | Endocardium structure | true | Inferred relationship | Some | 1 | |
Congenital endocardial fibroelastosis (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital endocardial fibroelastosis (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
A rare syndromic cardiac disease characterized by communicating hydrocephalus, endocardial fibroelastosis, and congenital cataracts. A history of upper respiratory infection in the mother during the first trimester of pregnancy and polyhydramnios in the third trimester has been associated. No evidence of toxoplasmosis, rubella, cytomegalovirus, herpes simplex virus, syphilis, and galactosemia is reported. There have been no further descriptions in the literature since 1995. | Is a | True | Congenital endocardial fibroelastosis (disorder) | Inferred relationship | Some |
This concept is not in any reference sets