FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

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
5069991000241119 embryotoxon fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Embryotoxon Is a Congenital structural abnormality of cornea true Inferred relationship Some
Embryotoxon Occurrence Congenital false Inferred relationship Some
Embryotoxon Finding site Corneal structure true Inferred relationship Some 1
Embryotoxon Finding site Structure of nervous system (body structure) false Inferred relationship Some
Embryotoxon Finding site Orbital region structure false Inferred relationship Some 1
Embryotoxon Associated morphology anomalie congénitale false Inferred relationship Some 1
Embryotoxon Associated morphology anomalie congénitale false Inferred relationship Some 1
Embryotoxon Occurrence Congenital false Inferred relationship Some
Embryotoxon Finding site Corneal structure false Inferred relationship Some 1
Embryotoxon Associated morphology anomalie congénitale false Inferred relationship Some 1
Embryotoxon Occurrence Congenital false Inferred relationship Some 2
Embryotoxon Associated morphology anomalie du développement false Inferred relationship Some 2
Embryotoxon Finding site Corneal structure false Inferred relationship Some 2
Embryotoxon Occurrence Congenital true Inferred relationship Some 1
Embryotoxon Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Embryotoxon 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 Inferred relationship Some
Axenfeld's anomaly Is a False Embryotoxon Inferred relationship Some
Posterior embryotoxon (disorder) Is a True Embryotoxon Inferred relationship Some

This concept is not in any reference sets

Back to Start