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253228006: Embryotoxon (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
377130019 Embryotoxon en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
643961010 Embryotoxon (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Embryotoxon morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
Embryotoxon Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Embryotoxon morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Embryotoxon survenue (attribut) congénital false Inferred relationship Some
Embryotoxon localisation d'une constatation (attribut) cornée (structure corporelle) false Inferred relationship Some 1
Embryotoxon morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Embryotoxon survenue (attribut) congénital false Inferred relationship Some 2
Embryotoxon morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
Embryotoxon localisation d'une constatation (attribut) cornée (structure corporelle) false Inferred relationship Some 2
Embryotoxon survenue (attribut) congénital false Inferred relationship Some
Embryotoxon localisation d'une constatation (attribut) cornée (structure corporelle) true Inferred relationship Some 1
Embryotoxon localisation d'une constatation (attribut) système nerveux false Inferred relationship Some
Embryotoxon localisation d'une constatation (attribut) Orbital region structure false Inferred relationship Some 1
Embryotoxon morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Embryotoxon survenue (attribut) congénital true Inferred relationship Some 1
Embryotoxon est un(e) (attribut) Congenital anomaly of cornea true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Axenfeld's anomaly est un(e) (attribut) False Embryotoxon Inferred relationship Some
Posterior embryotoxon (disorder) est un(e) (attribut) True Embryotoxon Inferred relationship Some
Anterior embryotoxon est un(e) (attribut) False Embryotoxon Inferred relationship Some

This concept is not in any reference sets

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