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


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2981458015 Hereditary retinal dystrophy primarily involving sensory retina en Synonym Active Entire term case insensitive SNOMED CT core module
2981465011 Inherited retinal dystrophy primarily involving sensory retina en Synonym Active Entire term case insensitive SNOMED CT core module
2981483015 Hereditary retinal dystrophy primarily involving sensory retina (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
Hereditary retinal dystrophy primarily involving sensory retina Is a Hereditary retinal dystrophy true Inferred relationship Existential restriction modifier
Hereditary retinal dystrophy primarily involving sensory retina Finding site Retinal structure false Inferred relationship Existential restriction modifier
Hereditary retinal dystrophy primarily involving sensory retina Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Hereditary retinal dystrophy primarily involving sensory retina 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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