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789675009: Complete achromatopsia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3791517011 Complete achromatopsia en Synonym Active Entire term case insensitive SNOMED CT core module
3791518018 Complete color blindness en Synonym Active Entire term case insensitive SNOMED CT core module
3791519014 Complete colour blindness en Synonym Active Entire term case insensitive SNOMED CT core module
3791520015 Complete achromatopsia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3791521016 Total colour blindness en Synonym Active Entire term case insensitive SNOMED CT core module
3791522011 Rod monochromatism en Synonym Active Entire term case insensitive SNOMED CT core module
3791523018 Total color blindness en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Complete achromatopsia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Complete achromatopsia Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Complete achromatopsia Is a Achromatopsia true Inferred relationship Existential restriction modifier
Complete achromatopsia Finding site Cone of retina true Inferred relationship Existential restriction modifier 1
Complete achromatopsia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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