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723828008: Autosomal recessive bestrophinopathy (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3426298018 Retinopathy Burgess Black type en Synonym Active Only initial character case insensitive SNOMED CT core module
3426299014 Autosomal recessive bestrophinopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3426300018 Autosomal recessive bestrophinopathy (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
Autosomal recessive bestrophinopathy Is a Hereditary retinal dystrophy true Inferred relationship Existential restriction modifier
Autosomal recessive bestrophinopathy Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal recessive bestrophinopathy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Autosomal recessive bestrophinopathy 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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