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719520001: Benign concentric annular macular dystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
3316671014 Benign concentric annular macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5402149010 Benign concentric annular macular dystrophy (BCAMD) is a progressive autosomal dominant macular dystrophy characterized by parafoveal hypopigmentation followed by a retinitis pigmentosa-like phenotype (nyctalopia and peripheral vision loss) with a bull's eye configuration. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402150010 Benign concentric annular macular dystrophy (BCAMD) is a progressive autosomal dominant macular dystrophy characterised by parafoveal hypopigmentation followed by a retinitis pigmentosa-like phenotype (nyctalopia and peripheral vision loss) with a bull's eye configuration. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3316670010 Benign concentric annular macular dystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3316670010 Benign concentric annular macular dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3316671014 Benign concentric annular macular dystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3316671014 Benign concentric annular macular dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3316672019 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 Entire term case sensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core
5402149010 Benign concentric annular macular dystrophy (BCAMD) is a progressive autosomal dominant macular dystrophy characterized by parafoveal hypopigmentation followed by a retinitis pigmentosa-like phenotype (nyctalopia and peripheral vision loss) with a bull's eye configuration. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402150010 Benign concentric annular macular dystrophy (BCAMD) is a progressive autosomal dominant macular dystrophy characterised by parafoveal hypopigmentation followed by a retinitis pigmentosa-like phenotype (nyctalopia and peripheral vision loss) with a bull's eye configuration. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
601511000274114 Anuläre benigne konzentrische Makuladystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3451161001000111 Makuladystrophie, anuläre benigne konzentrische de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1007731000172119 dystrophie maculaire annulaire concentrique bénigne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1007731000172119 dystrophie maculaire annulaire concentrique bénigne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
601511000274114 Anuläre benigne konzentrische Makuladystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3451161001000111 Makuladystrophie, anuläre benigne konzentrische de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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