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1141882007: Congenital endocardial fibroelastosis (disorder)


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


1 descendants. Search Descendants:

Expanded Value Set


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

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