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715430001: Embryofetopathy caused by indomethacin (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3302597019 Fetal indomethacin syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3302598012 Foetal indomethacin syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3302602014 Embryofetopathy caused by indomethacin (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3302603016 Embryofetopathy caused by indomethacin en Synonym Active Entire term case insensitive SNOMED CT core module
3302622013 Indomethacin embryofetopathy en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Embryofetopathy caused by indomethacin Is a Drug-related disorder false Inferred relationship Existential restriction modifier
Embryofetopathy caused by indomethacin Is a Congenital malformation syndrome due to known exogenous cause false Inferred relationship Existential restriction modifier
Embryofetopathy caused by indomethacin Is a Disorder of fetal structure false Inferred relationship Existential restriction modifier
Embryofetopathy caused by indomethacin Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Embryofetopathy caused by indomethacin Causative agent Indometacin true Inferred relationship Existential restriction modifier 1
Embryofetopathy caused by indomethacin Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Embryofetopathy caused by indomethacin Finding site Fetal structure true Inferred relationship Existential restriction modifier 1
Embryofetopathy caused by indomethacin Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Embryofetopathy caused by indomethacin Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Embryofetopathy caused by indomethacin Is a Congenital malformation syndrome true Inferred relationship Existential restriction modifier
Embryofetopathy caused by indomethacin Is a Disorder by body site false Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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