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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
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
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 Only initial character 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 Only initial character 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
94545017 Complete color blindness en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
94545017 Complete color blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
94546016 Achromatism en Synonym (core metadata concept) Active Only initial character 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
497710018 Complete colour blindness en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
497710018 Complete colour blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
795410010 Achromatopsia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
795410010 Achromatopsia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1216754017 Total colour blindness en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1216754017 Total colour blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1218244014 Total color blindness en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1218244014 Total color blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
645441000274117 Achromatismus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3443881001000112 Achromatopsie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
978521000172112 achromatopsie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
995221000172114 ACHM - achromatopsie fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
978521000172112 achromatopsie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
995221000172114 ACHM - achromatopsie fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
645441000274117 Achromatismus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3443881001000112 Achromatopsie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Achromatopsia Is a Congenital color blindness true Inferred relationship Existential restriction modifier (core metadata concept)
Achromatopsia Is a Hereditary retinal dystrophy (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Achromatopsia Is a Hereditary disorder of the visual system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Achromatopsia Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept)
Achromatopsia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Achromatopsia Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 1
Achromatopsia Interprets Vision observable (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Achromatopsia Interprets Visual function (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Achromatopsia Has interpretation Abnormal false Inferred relationship Existential restriction modifier (core metadata concept) 1
Achromatopsia Interprets Visual function (observable entity) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Achromatopsia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Achromatopsia Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Achromatopsia Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 2
Achromatopsia Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Achromatopsia Is a Congenital anomaly of retina true Inferred relationship Existential restriction modifier (core metadata concept)
Achromatopsia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Achromatopsia Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Achromatopsia Is a Cone dystrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Achromatopsia Finding site Cone of retina true Inferred relationship Existential restriction modifier (core metadata concept) 1
Achromatopsia Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Achromatopsia Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Rod monochromatism Is a False Achromatopsia Inferred relationship Existential restriction modifier (core metadata concept)
Cone monochromatism Is a False Achromatopsia Inferred relationship Existential restriction modifier (core metadata concept)
Complete achromatopsia Is a True Achromatopsia Inferred relationship Existential restriction modifier (core metadata concept)
Incomplete achromatopsia (disorder) Is a True Achromatopsia Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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