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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
5403440010 A rare teratogenic disorder due to acitretin or etretinate exposure 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
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
5403440010 A rare teratogenic disorder due to acitretin or etretinate exposure 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
3455021001000119 Acitretin/Etretinat-Embryofetopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6105781000241110 embryopathie causée par un rétinoïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6105781000241110 embryopathie causée par un rétinoïde fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3455021001000119 Acitretin/Etretinat-Embryofetopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinoid embryopathy Is a Congenital malformation caused by cytotoxic agents (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Retinoid embryopathy Is a Disorder of fetal structure true Inferred relationship Existential restriction modifier (core metadata concept)
Retinoid embryopathy Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinoid embryopathy Causative agent (attribute) Retinoid (substance) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinoid embryopathy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinoid embryopathy Finding site Fetal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinoid embryopathy Is a Congenital malformation syndrome due to known exogenous cause false Inferred relationship Existential restriction modifier (core metadata concept)
Retinoid embryopathy Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinoid embryopathy Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinoid embryopathy Is a Congenital malformation syndrome false Inferred relationship Existential restriction modifier (core metadata concept)
Retinoid embryopathy Occurrence Fetal period (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Retinoid embryopathy Is a Fetus with drug damage true Inferred relationship Existential restriction modifier (core metadata concept)
Retinoid embryopathy Is a Fetal disorder caused by chemicals (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Embryopathy caused by acitretin (disorder) Is a True Retinoid embryopathy Inferred relationship Existential restriction modifier (core metadata concept)
Embryopathy caused by isotretinoin (disorder) Is a True Retinoid embryopathy Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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