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1208840000: Incomplete achromatopsia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5013174010 Incomplete achromatopsia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5013175011 Incomplete achromatopsia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5013174010 Incomplete achromatopsia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5013175011 Incomplete achromatopsia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
520211000274117 Inkomplette Farbenblindheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
592651000274112 Inkomplette Achromatopsie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
520211000274117 Inkomplette Farbenblindheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
592651000274112 Inkomplette Achromatopsie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Incomplete achromatopsia (disorder) Is a Achromatopsia true Inferred relationship Existential restriction modifier (core metadata concept)
Incomplete achromatopsia (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Incomplete achromatopsia (disorder) Finding site Cone of retina true Inferred relationship Existential restriction modifier (core metadata concept) 1
Incomplete achromatopsia (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Incomplete achromatopsia (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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