36871005: Retinoic acid embryopathy (disorder)

Status: retired, Not 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

2816635015 Foetal vitamin A syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

486569018 Fetal vitamin A syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

486570017 Congenital malformation due to vitamin A en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

61500013 Retinoic acid embryopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

68341000077117 embryopathie causée par l'acide rétinoïque fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

690611000077115 embryopathie causée par l'acide rétinoïque (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

768673017 Retinoic acid embryopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Retinoic acid embryopathy	est un(e) (attribut)	Drug-related disorder	false	Inferred relationship	Some
Retinoic acid embryopathy	Causative agent	Isotretinoin (substance)	false	Inferred relationship	Some
Retinoic acid embryopathy	Causative agent	Tretinoin (substance)	false	Inferred relationship	Some
Retinoic acid embryopathy	est un(e) (attribut)	Multiple malformation syndrome due to non-infectious environmental agents (disorder)	false	Inferred relationship	Some
Retinoic acid embryopathy	est un(e) (attribut)	Congenital malformation syndromes due to known exogenous causes	false	Inferred relationship	Some
Retinoic acid embryopathy	morphologie associée (attribut)	Congenital malformation	false	Inferred relationship	Some
Retinoic acid embryopathy	est un(e) (attribut)	Drug-related disorder	false	Inferred relationship	Some
Retinoic acid embryopathy	est un(e) (attribut)	Congenital malformation syndrome due to known exogenous cause	false	Inferred relationship	Some
Retinoic acid embryopathy	est un(e) (attribut)	Drug-related disorder	false	Inferred relationship	Some
Retinoic acid embryopathy	survenue (attribut)	congénital	false	Inferred relationship	Some	1
Retinoic acid embryopathy	morphologie associée (attribut)	Developmental abnormality	false	Inferred relationship	Some	1
Retinoic acid embryopathy	survenue (attribut)	congénital	false	Inferred relationship	Some
Retinoic acid embryopathy	Causative agent	Product containing tretinoin (medicinal product)	false	Inferred relationship	Some
Retinoic acid embryopathy	Causative agent	Product containing isotretinoin (medicinal product)	false	Inferred relationship	Some
Retinoic acid embryopathy	Causative agent	Environmental agent	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

Description inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)