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722066001: Oligocone trichromacy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3330453012 Oligocone trichromacy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3330454018 Oligocone trichromacy en Synonym Active Entire term case insensitive SNOMED CT core module
3330455017 Oligocone syndrome 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
Oligocone trichromacy Is a Hereditary retinal dystrophy true Inferred relationship Existential restriction modifier
Oligocone trichromacy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Oligocone trichromacy Finding site Retinal structure 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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