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715430001: embryofoetopathie door indometacine (aandoening)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3302597019 Fetal indomethacin syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302598012 Foetal indomethacin syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302602014 Embryofetopathy caused by indomethacin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302603016 Embryofetopathy caused by indomethacin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3302622013 Indomethacin embryofetopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6628611000146110 embryofoetopathie door indometacine nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6628641000146111 embryofoetopathie door indometacine (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3302600018 A group of symptoms which may be observed in the fetus or newborn when the mother has taken indomethacin, a nonsteroidal anti-inflammatory drug during pregnancy. The drug crosses the human placenta readily throughout gestation, but its effects on the embryo/fetus vary according to the stage of pregnancy. 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
Embryofetopathy caused by indomethacin (disorder) Is a aandoening bij drug of geneesmiddel (aandoening) false Inferred relationship Some
Embryofetopathy caused by indomethacin (disorder) Is a Congenital malformation syndrome due to known exogenous cause false Inferred relationship Some
Embryofetopathy caused by indomethacin (disorder) Is a Disorder of fetal structure false Inferred relationship Some
Embryofetopathy caused by indomethacin (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 1
Embryofetopathy caused by indomethacin (disorder) Causative agent Indometacin true Inferred relationship Some 1
Embryofetopathy caused by indomethacin (disorder) Occurrence Congenital true Inferred relationship Some 1
Embryofetopathy caused by indomethacin (disorder) Finding site Fetal structure true Inferred relationship Some 1
Embryofetopathy caused by indomethacin (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Embryofetopathy caused by indomethacin (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Embryofetopathy caused by indomethacin (disorder) Is a Congenital malformation syndrome (disorder) true Inferred relationship Some
Embryofetopathy caused by indomethacin (disorder) Is a aandoening ingedeeld naar anatomische of verworven lichaamsstructuur (aandoening) false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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