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417604002: syndrome d'Axenfeld-Rieger (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2547474018 Axenfeld-Rieger syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2549818010 Axenfeld-Rieger syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3800347015 Axenfeld syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
654301000241113 syndrome d'Axenfeld-Rieger (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
898051000172111 syndrome d'Axenfeld fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
960601000172111 syndrome d'Axenfeld-Rieger fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Axenfeld-Rieger syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Axenfeld-Rieger syndrome (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
Axenfeld-Rieger syndrome (disorder) est un(e) (attribut) Congenital anomaly of anterior chamber of eye true Inferred relationship Some
Axenfeld-Rieger syndrome (disorder) est un(e) (attribut) Irido-corneal dysgenesis false Inferred relationship Some
Axenfeld-Rieger syndrome (disorder) survenue (attribut) congénital false Inferred relationship Some
Axenfeld-Rieger syndrome (disorder) localisation d'une constatation (attribut) Anterior chamber of eye structure false Inferred relationship Some 1
Axenfeld-Rieger syndrome (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Axenfeld-Rieger syndrome (disorder) localisation d'une constatation (attribut) segment antérieur du globe oculaire (structure corporelle) false Inferred relationship Some 2
Axenfeld-Rieger syndrome (disorder) morphologie associée (attribut) Congenital developmental anomaly (morphologic abnormality) false Inferred relationship Some 2
Axenfeld-Rieger syndrome (disorder) localisation d'une constatation (attribut) Anterior chamber of eye structure true Inferred relationship Some 1
Axenfeld-Rieger syndrome (disorder) localisation d'une constatation (attribut) segment antérieur du globe oculaire (structure corporelle) false Inferred relationship Some 2
Axenfeld-Rieger syndrome (disorder) morphologie associée (attribut) Congenital developmental anomaly (morphologic abnormality) false Inferred relationship Some 2
Axenfeld-Rieger syndrome (disorder) morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Axenfeld-Rieger syndrome (disorder) survenue (attribut) congénital false Inferred relationship Some 3
Axenfeld-Rieger syndrome (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 3
Axenfeld-Rieger syndrome (disorder) localisation d'une constatation (attribut) Anterior chamber of eye structure false Inferred relationship Some 3
Axenfeld-Rieger syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Irido-trabecular dysgenesis est un(e) (attribut) True Axenfeld-Rieger syndrome (disorder) Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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