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38323006: Fetal warfarin syndrome (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
64136018 Fetal warfarin syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
773275016 Fetal warfarin syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1229413014 Dysmorphism due to warfarin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3011848011 Foetal warfarin syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
64136018 Fetal warfarin syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
64136018 Fetal warfarin syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
773275016 Fetal warfarin syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
773275016 Fetal warfarin syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1229413014 Dysmorphism due to warfarin en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1229413014 Dysmorphism due to warfarin en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3011848011 Foetal warfarin syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3011848011 Foetal warfarin syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3408691001000111 Vitamin K-Antagonisten-Embryopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4515141000241117 syndrome d'intoxication foetale à la warfarine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4515141000241117 syndrome d'intoxication foetale à la warfarine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3408691001000111 Vitamin K-Antagonisten-Embryopathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fetal warfarin syndrome Is a Multiple malformation syndrome due to non-infectious environmental agents false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Is a Congenital malformation syndromes due to known exogenous causes false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Causative agent (attribute) Product containing warfarin (medicinal product) false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Causative agent (attribute) Environmental agent false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Is a trouble causé par un médicament false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Is a fœtus ou nouveau-né affecté par le transfert placentaire ou mammaire d'anticoagulant false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Is a anomalies fœtales congénitales false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Causative agent (attribute) Warfarin (substance) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Fetal warfarin syndrome Occurrence Neonatal false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Occurrence Fetal period (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Occurrence période périnatale false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Finding site Fetal structure false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Is a Congenital malformation syndrome due to known exogenous cause false Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Occurrence Fetal or neonatal period false Inferred relationship Existential restriction modifier (core metadata concept) 3
Fetal warfarin syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Fetal warfarin syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Fetal warfarin syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Fetal warfarin syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Fetal warfarin syndrome Is a Fetus with drug damage true Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Finding site Fetal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Fetal warfarin syndrome Occurrence Fetal period (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Fetal warfarin syndrome Causative agent (attribute) Warfarin (substance) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Fetal warfarin syndrome Is a Disorder of fetal structure true Inferred relationship Existential restriction modifier (core metadata concept)
Fetal warfarin syndrome Occurrence Fetal or neonatal period false Inferred relationship Existential restriction modifier (core metadata concept) 2
Fetal warfarin syndrome Is a Fetal disorder caused by chemicals (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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