FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

719520001: Benign concentric annular macular dystrophy (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3316670010 Benign concentric annular macular dystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3316671014 Benign concentric annular macular dystrophy en Synonym Active Case insensitive SNOMED CT core
4361404018 A progressive autosomal dominant macular dystrophy with characteristics of parafoveal hypopigmentation followed by a retinitis pigmentosa-like phenotype (nyctalopia and peripheral vision loss) with a bull's eye configuration. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Benign concentric annular macular dystrophy Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Benign concentric annular macular dystrophy Is a Hereditary macular dystrophy true Inferred relationship Some
Benign concentric annular macular dystrophy Finding site Macula lutea structure false Inferred relationship Some
Benign concentric annular macular dystrophy Associated morphology Dystrophy false Inferred relationship Some 2
Benign concentric annular macular dystrophy Finding site Retinal structure false Inferred relationship Some 2
Benign concentric annular macular dystrophy Associated morphology Dystrophy true Inferred relationship Some 1
Benign concentric annular macular dystrophy Finding site Macula lutea 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

Back to Start