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232061009: cécité nocturne congénitale stationnaire (trouble)


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
2619554012 CSNB - Congenital stationary night blindness en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
347712011 Congenital stationary night blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
620077018 Congenital stationary night blindness (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
699391000077112 cécité nocturne congénitale stationnaire (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
76871000077113 cécité nocturne congénitale stationnaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
953061000172117 cécité nocturne stationnaire congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
953361000172115 héméralopie congénitale essentielle fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital stationary night blindness est un(e) (attribut) Night blindness true Inferred relationship Some
Congenital stationary night blindness Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital stationary night blindness est un(e) (attribut) Congenital anomaly of retina (disorder) true Inferred relationship Some
Congenital stationary night blindness morphologie associée (attribut) Dystrophy (morphologic abnormality) true Inferred relationship Some 1
Congenital stationary night blindness est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Congenital stationary night blindness est un(e) (attribut) Congenital anomaly of eye false Inferred relationship Some
Congenital stationary night blindness survenue (attribut) congénital false Inferred relationship Some
Congenital stationary night blindness est un(e) (attribut) Congenital disease false Inferred relationship Some
Congenital stationary night blindness est un(e) (attribut) Hereditary retinal dystrophy true Inferred relationship Some
Congenital stationary night blindness survenue (attribut) congénital true Inferred relationship Some 1
Congenital stationary night blindness localisation d'une constatation (attribut) structure de la rétine true Inferred relationship Some 1
Congenital stationary night blindness localisation d'une constatation (attribut) structure de la rétine false Inferred relationship Some
Congenital stationary night blindness morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 2
Congenital stationary night blindness localisation d'une constatation (attribut) structure de la rétine false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Oguchi's disease est un(e) (attribut) True Congenital stationary night blindness 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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