FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

890202007: 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
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
6096481000241115 embryopathie causée par l'acitrétine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6096481000241115 embryopathie causée par l'acitrétine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Embryopathy caused by acitretin (disorder) Is a Retinoid embryopathy true Inferred relationship Existential restriction modifier (core metadata concept)
Embryopathy caused by acitretin (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Embryopathy caused by acitretin (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Embryopathy caused by acitretin (disorder) Causative agent (attribute) Acitretin (substance) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Embryopathy caused by acitretin (disorder) Occurrence Fetal period (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start