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890202007: embryopathie door acitretine (aandoening)

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
12133171000146115 embryopathie door acitretine nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12133181000146118 embryopathie door acitretine (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
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

0 descendants.

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 Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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