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715430001: Embryofetopathy caused by indomethacin (disorder)

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 Reference Sets
3302597019 Fetal indomethacin syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
3302598012 Foetal indomethacin syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
3302602014 Embryofetopathy caused by indomethacin (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
3302603016 Embryofetopathy caused by indomethacin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
3302622013 Indomethacin embryofetopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation 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 GB English: Preferred (foundation metadata concept)
3872301000052115 embryopati-fetopati orsakad av indometacin sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept) Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept)

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Embryofetopathy caused by indomethacin (disorder) Is a Drug-related disorder true Inferred relationship Some
Embryofetopathy caused by indomethacin (disorder) Is a medfött missbildningssyndrom orsakat av känd exogen faktor 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 Developmental anomaly (morphologic abnormality) 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 Disorder by body site (disorder) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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