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417395001: Congenital hereditary endothelial dystrophy type 2 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2553628017 Congenital hereditary endothelial dystrophy, autosomal recessive form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3776017011 Congenital hereditary endothelial dystrophy type 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3776018018 CHED II - Congenital hereditary endothelial dystrophy II en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3776019014 Congenital hereditary endothelial dystrophy type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2546082019 Congenital hereditary endothelial dystrophy,CHED 2 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2548354014 Congenital hereditary endothelial dystrophy,CHED 2 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2553628017 Congenital hereditary endothelial dystrophy, autosomal recessive form en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2553628017 Congenital hereditary endothelial dystrophy, autosomal recessive form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2913936013 Congenital hereditary endothelial dystrophy, 2 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2913936013 Congenital hereditary endothelial dystrophy, 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2915201016 Congenital hereditary endothelial dystrophy, 2 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2915201016 Congenital hereditary endothelial dystrophy, 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3776017011 Congenital hereditary endothelial dystrophy type 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3776018018 CHED II - Congenital hereditary endothelial dystrophy II en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3776019014 Congenital hereditary endothelial dystrophy type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
537171000274119 CHED2 - Kongenitale hereditäre Endotheldystrophie, Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
574081000274112 Kongenitale hereditäre Endotheldystrophie, Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
881441000172112 CHED (congenital hereditary endothelial dystrophy) autosomique récessive fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1021111000172114 dystrophie endothéliale congénitale héréditaire type II fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
881441000172112 CHED (congenital hereditary endothelial dystrophy) autosomique récessive fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1021111000172114 dystrophie endothéliale congénitale héréditaire type II fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
537171000274119 CHED2 - Kongenitale hereditäre Endotheldystrophie, Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
574081000274112 Kongenitale hereditäre Endotheldystrophie, Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3428591001000118 Endotheldystrophie, hereditäre kongenitale, Typ II 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
Congenital hereditary endothelial dystrophy type 2 (disorder) Is a Congenital hereditary endothelial dystrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hereditary endothelial dystrophy type 2 (disorder) Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hereditary endothelial dystrophy type 2 (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hereditary endothelial dystrophy type 2 (disorder) Finding site Chromosome pair 20 false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hereditary endothelial dystrophy type 2 (disorder) Finding site Corneal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hereditary endothelial dystrophy type 2 (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hereditary endothelial dystrophy type 2 (disorder) Finding site Structure of corneal endothelium false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hereditary endothelial dystrophy type 2 (disorder) Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hereditary endothelial dystrophy type 2 (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hereditary endothelial dystrophy type 2 (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hereditary endothelial dystrophy type 2 (disorder) Finding site Structure of corneal endothelium true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hereditary endothelial dystrophy type 2 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hereditary endothelial dystrophy type 2 (disorder) Finding site Chromosome pair 20 true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hereditary endothelial dystrophy type 2 (disorder) Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hereditary endothelial dystrophy type 2 (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hereditary endothelial dystrophy type 2 (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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