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770594005: Retinal macular dystrophy type 2 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3701485013 Retinal macular dystrophy type 2 en Synonym Active Entire term case insensitive SNOMED CT core module
3701486014 MCDR2 - retinal macular dystrophy type 2 en Synonym Active Entire term case sensitive SNOMED CT core module
3701487017 Retinal macular dystrophy type 2 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinal macular dystrophy type 2 Is a Hereditary macular dystrophy true Inferred relationship Existential restriction modifier
Retinal macular dystrophy type 2 Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Retinal macular dystrophy type 2 Finding site Macula lutea structure true Inferred relationship Existential restriction modifier 1
Retinal macular dystrophy type 2 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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