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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
5785481000172119 embryotoxon congénital fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
8948751000172119 embryotoxon fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
8988561000172115 arc de coloration blanche ou grisâtre autour de l'iris fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4358611000172117 embryotoxon nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Embryotoxon (disorder) Is a Congenital anomaly of cornea true Inferred relationship Some
Embryotoxon (disorder) Occurrence Congenital false Inferred relationship Some
Embryotoxon (disorder) Finding site Corneal structure true Inferred relationship Some 1
Embryotoxon (disorder) Finding site Structure of nervous system (body structure) false Inferred relationship Some
Embryotoxon (disorder) Finding site Orbital region structure false Inferred relationship Some 1
Embryotoxon (disorder) Associated morphology Congenital anomaly false Inferred relationship Some 1
Embryotoxon (disorder) Associated morphology Congenital anomaly false Inferred relationship Some 1
Embryotoxon (disorder) Occurrence Congenital false Inferred relationship Some
Embryotoxon (disorder) Finding site Corneal structure false Inferred relationship Some 1
Embryotoxon (disorder) Associated morphology Congenital anomaly false Inferred relationship Some 1
Embryotoxon (disorder) Occurrence Congenital false Inferred relationship Some 2
Embryotoxon (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 2
Embryotoxon (disorder) Finding site Corneal structure false Inferred relationship Some 2
Embryotoxon (disorder) Occurrence Congenital true Inferred relationship Some 1
Embryotoxon (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Embryotoxon (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

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

This concept is not in any reference sets

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