890202007: Embryopathy caused by acitretin (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Fetal finding\Fetal disorder\...

\Disorder of fetal structure\Embryopathy caused by retinoid (disorder)\Embryopathy caused by acitretin (disorder)

\Foetal disorder caused by chemicals\Embryopathy caused by retinoid (disorder)\Embryopathy caused by acitretin (disorder)

\Fetus with drug damage\Embryopathy caused by retinoid (disorder)\Embryopathy caused by acitretin (disorder)

\Disease\Disorder of foetus and/or newborn\Fetal disorder\Disorder of fetal structure\Embryopathy caused by retinoid (disorder)\Embryopathy caused by acitretin (disorder)
\Disease\Disorder of foetus and/or newborn\Fetal disorder\Foetal disorder caused by chemicals\Embryopathy caused by retinoid (disorder)\Embryopathy caused by acitretin (disorder)
\Disease\Disorder of foetus and/or newborn\Fetal disorder\Fetus with drug damage\Embryopathy caused by retinoid (disorder)\Embryopathy caused by acitretin (disorder)
\Disease\Developmental disorder\Disorder of fetal structure\Embryopathy caused by retinoid (disorder)\Embryopathy caused by acitretin (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4009842013 Foetal acitretin syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4009844014 Acitretin embryofoetopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4009845010 Acitretin embryopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4009846011 Fetal acitretin syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4009847019 Acitretin embryofetopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4013006018 Embryopathy caused by acitretin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4013007010 Embryopathy caused by acitretin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

4009848012 A rare teratogenic disorder due to acitretin 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

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Embryopathy caused by acitretin (disorder)	Is a	Embryopathy caused by retinoid (disorder)	true	Inferred relationship	Some
Embryopathy caused by acitretin (disorder)	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1
Embryopathy caused by acitretin (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Embryopathy caused by acitretin (disorder)	Causative agent	Acitretin (substance)	true	Inferred relationship	Some	1
Embryopathy caused by acitretin (disorder)	Occurrence	Fetal period	true	Inferred relationship	Some	1

Inbound Relationships

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This concept is not in any reference sets