416633008: congenitale hereditaire endotheeldystrofie type 1 (aandoening)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jul 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3644846012 Congenital hereditary endothelial dystrophy type 1 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3644847015 Congenital hereditary endothelial dystrophy autosomal dominant form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3644848013 Congenital hereditary endothelial dystrophy type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3644852013 CHED1 - congenital hereditary endothelial dystrophy type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

6573541000146114 congenitale hereditaire endotheeldystrofie type 1 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6573551000146112 congenitale hereditaire endotheeldystrofie type 1 (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
congenitale hereditaire endotheeldystrofie type 1	Is a	Congenital hereditary endothelial dystrophy (disorder)	false	Inferred relationship	Some
congenitale hereditaire endotheeldystrofie type 1	Associated morphology	congenitale anomalie (afwijkende morfologie)	false	Inferred relationship	Some	1
congenitale hereditaire endotheeldystrofie type 1	Finding site	Corneal structure	false	Inferred relationship	Some	1
congenitale hereditaire endotheeldystrofie type 1	Finding site	Chromosome pair 20	false	Inferred relationship	Some	1
congenitale hereditaire endotheeldystrofie type 1	Occurrence	Congenital	false	Inferred relationship	Some
congenitale hereditaire endotheeldystrofie type 1	Associated morphology	Dystrophy	false	Inferred relationship	Some	1
congenitale hereditaire endotheeldystrofie type 1	Associated morphology	Dystrophy	false	Inferred relationship	Some	2
congenitale hereditaire endotheeldystrofie type 1	Finding site	Structure of corneal endothelium	false	Inferred relationship	Some	2
congenitale hereditaire endotheeldystrofie type 1	Associated morphology	congenitale anomalie (afwijkende morfologie)	false	Inferred relationship	Some
congenitale hereditaire endotheeldystrofie type 1	Associated morphology	Dystrophy	false	Inferred relationship	Some	1
congenitale hereditaire endotheeldystrofie type 1	Finding site	Structure of corneal endothelium	false	Inferred relationship	Some	1
congenitale hereditaire endotheeldystrofie type 1	Occurrence	Congenital	false	Inferred relationship	Some	2
congenitale hereditaire endotheeldystrofie type 1	Finding site	Chromosome pair 20	false	Inferred relationship	Some	2
congenitale hereditaire endotheeldystrofie type 1	Associated morphology	Cellular AND/OR subcellular abnormality	false	Inferred relationship	Some	2
congenitale hereditaire endotheeldystrofie type 1	Is a	Autosomal dominant hereditary disorder	false	Inferred relationship	Some
congenitale hereditaire endotheeldystrofie type 1	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)