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725287006: Embryopathy caused by retinoid (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3440735015 Embryopathy caused by retinoid (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3440736019 Retinoid embryopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3440737011 Embryopathy caused by retinoid en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3440738018 A teratogenic disorder caused by exposure to retinoid during the first trimester of pregnancy, carrying a risk of fetal malformations of approximately 20%, including central nervous system, craniofacial, ear, thymic, cardiac and limb anomalies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Embryopathy caused by retinoid (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
Embryopathy caused by retinoid (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Embryopathy caused by retinoid (disorder) est un(e) (attribut) Congenital malformation syndrome (disorder) false Inferred relationship Some
Embryopathy caused by retinoid (disorder) survenue (attribut) période fœtale true Inferred relationship Some 1
Embryopathy caused by retinoid (disorder) est un(e) (attribut) Fetus with drug damage true Inferred relationship Some
Embryopathy caused by retinoid (disorder) est un(e) (attribut) malformation congénitale causée par des agents cytotoxiques false Inferred relationship Some
Embryopathy caused by retinoid (disorder) est un(e) (attribut) Disorder of fetal structure true Inferred relationship Some
Embryopathy caused by retinoid (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 1
Embryopathy caused by retinoid (disorder) Causative agent Retinoid (substance) true Inferred relationship Some 1
Embryopathy caused by retinoid (disorder) survenue (attribut) congénital false Inferred relationship Some 1
Embryopathy caused by retinoid (disorder) localisation d'une constatation (attribut) Fetal structure false Inferred relationship Some 1
Embryopathy caused by retinoid (disorder) est un(e) (attribut) Congenital malformation syndrome due to known exogenous cause false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Embryopathy caused by acitretin (disorder) est un(e) (attribut) True Embryopathy caused by retinoid (disorder) Inferred relationship Some

This concept is not in any reference sets

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