FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

773727009: Autosomal dominant rhegmatogenous retinal detachment (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
3726004011 Autosomal dominant rhegmatogenous retinal detachment (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3726005012 Autosomal dominant rhegmatogenous retinal detachment 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
Autosomal dominant rhegmatogenous retinal detachment Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Autosomal dominant rhegmatogenous retinal detachment Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant rhegmatogenous retinal detachment Is a Rhegmatogenous retinal detachment true Inferred relationship Existential restriction modifier
Autosomal dominant rhegmatogenous retinal detachment Finding site Retinal structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant rhegmatogenous retinal detachment Associated morphology Separation true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start