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698848005: Hereditary retinal dystrophy primarily involving sensory retina (disorder)


Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2981458015 Hereditary retinal dystrophy primarily involving sensory retina en Synonym Active Case insensitive SNOMED CT core
2981465011 Inherited retinal dystrophy primarily involving sensory retina en Synonym Active Case insensitive SNOMED CT core
2981483015 Hereditary retinal dystrophy primarily involving sensory retina (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary retinal dystrophy primarily involving sensory retina Is a Hereditary retinal dystrophy true Inferred relationship Some
Hereditary retinal dystrophy primarily involving sensory retina Finding site Retinal structure false Inferred relationship Some
Hereditary retinal dystrophy primarily involving sensory retina Associated morphology Dystrophy true Inferred relationship Some 1
Hereditary retinal dystrophy primarily involving sensory retina Finding site Retinal structure 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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