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253228006: embryotoxon (aandoening)


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
8364681000146116 embryotoxon nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8364691000146119 embryotoxon (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained 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 structural abnormality 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 congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 1
Embryotoxon (disorder) Associated morphology congenitale anomalie (afwijkende morfologie) 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 congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 1
Embryotoxon (disorder) Occurrence Congenital false Inferred relationship Some 2
Embryotoxon (disorder) Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) 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
embryotoxon anterior 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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