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789675009: Complete achromatopsia (disorder)


Status: current, Primitive. Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

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


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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