FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

56852002: Achromatopsia (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
443821000241112 achromatopsie (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
795410010 Achromatopsia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
94543012 Achromatopsia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
94544018 Monochromatism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
94546016 Achromatism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
978521000172112 achromatopsie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
995221000172114 ACHM - achromatopsie 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
achromatopsie (trouble) est un(e) (attribut) Congenital anomaly of retina (disorder) true Inferred relationship Some
achromatopsie (trouble) est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
achromatopsie (trouble) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
achromatopsie (trouble) est un(e) (attribut) Cone dystrophy true Inferred relationship Some
achromatopsie (trouble) localisation d'une constatation (attribut) Cone of retina true Inferred relationship Some 1
achromatopsie (trouble) morphologie associée (attribut) Dystrophy (morphologic abnormality) true Inferred relationship Some 1
achromatopsie (trouble) est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
achromatopsie (trouble) est un(e) (attribut) Congenital color blindness true Inferred relationship Some
achromatopsie (trouble) est un(e) (attribut) Hereditary retinal dystrophy false Inferred relationship Some
achromatopsie (trouble) est un(e) (attribut) Hereditary disorder of the visual system false Inferred relationship Some
achromatopsie (trouble) survenue (attribut) congénital false Inferred relationship Some
achromatopsie (trouble) a pour interprétation (attribut) anormal false Inferred relationship Some 1
achromatopsie (trouble) interprète (attribut) entité observable de la vision false Inferred relationship Some 1
achromatopsie (trouble) interprète (attribut) Visual function (observable entity) false Inferred relationship Some 1
achromatopsie (trouble) a pour interprétation (attribut) anormal false Inferred relationship Some 1
achromatopsie (trouble) interprète (attribut) Visual function (observable entity) false Inferred relationship Some 1
achromatopsie (trouble) survenue (attribut) congénital true Inferred relationship Some 1
achromatopsie (trouble) localisation d'une constatation (attribut) structure de la rétine false Inferred relationship Some 1
achromatopsie (trouble) morphologie associée (attribut) Dystrophy (morphologic abnormality) false Inferred relationship Some 2
achromatopsie (trouble) localisation d'une constatation (attribut) structure de la rétine false Inferred relationship Some 2
achromatopsie (trouble) localisation d'une constatation (attribut) structure de la rétine false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Complete achromatopsia est un(e) (attribut) True achromatopsie (trouble) Inferred relationship Some
Incomplete achromatopsia est un(e) (attribut) True achromatopsie (trouble) Inferred relationship Some
Cone monochromatism est un(e) (attribut) False achromatopsie (trouble) Inferred relationship Some
Rod monochromatism est un(e) (attribut) False achromatopsie (trouble) Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

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)

GB English

US English

Back to Start