FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

417651000: Congenital hereditary endothelial dystrophy (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
2547521014 Congenital hereditary endothelial dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2549868019 Congenital hereditary endothelial dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2554123017 CHED-congenital hereditary endothelial dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5874501000241111 CHED - congenital hereditary endothelial dystrophy fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5874511000241113 dystrophie congénitale héréditaire de l'endothélium cornéen fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
537651000274115 CHED - Kongenitale hereditäre Endotheldystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
574331000274110 Kongenitale hereditäre Endotheldystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hereditary endothelial dystrophy (disorder) Is a Hereditary corneal dystrophy true Inferred relationship Some
Congenital hereditary endothelial dystrophy (disorder) Is a Anomaly of chromosome pair 20 true Inferred relationship Some
Congenital hereditary endothelial dystrophy (disorder) Is a Corneal endothelial dystrophy (disorder) true Inferred relationship Some
Congenital hereditary endothelial dystrophy (disorder) Associated morphology Dystrophy false Inferred relationship Some 1
Congenital hereditary endothelial dystrophy (disorder) Occurrence Congenital false Inferred relationship Some
Congenital hereditary endothelial dystrophy (disorder) Finding site Chromosome pair 20 false Inferred relationship Some 1
Congenital hereditary endothelial dystrophy (disorder) Finding site Corneal structure false Inferred relationship Some 1
Congenital hereditary endothelial dystrophy (disorder) Associated morphology anomalie congénitale false Inferred relationship Some 1
Congenital hereditary endothelial dystrophy (disorder) Is a Corneal degeneration (disorder) false Inferred relationship Some
Congenital hereditary endothelial dystrophy (disorder) Associated morphology Dystrophy false Inferred relationship Some 2
Congenital hereditary endothelial dystrophy (disorder) Finding site Structure of corneal endothelium false Inferred relationship Some 2
Congenital hereditary endothelial dystrophy (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Congenital hereditary endothelial dystrophy (disorder) Finding site Structure of corneal endothelium true Inferred relationship Some 1
Congenital hereditary endothelial dystrophy (disorder) Associated morphology anomalie congénitale false Inferred relationship Some
Congenital hereditary endothelial dystrophy (disorder) Occurrence Congenital true Inferred relationship Some 2
Congenital hereditary endothelial dystrophy (disorder) Finding site Chromosome pair 20 true Inferred relationship Some 2
Congenital hereditary endothelial dystrophy (disorder) Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Some 2
Congenital hereditary endothelial dystrophy (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital hereditary endothelial dystrophy (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Congenital hereditary endothelial dystrophy (disorder) Is a Congenital malformation true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
dystrophie endothéliale congénitale héréditaire type I Is a False Congenital hereditary endothelial dystrophy (disorder) Inferred relationship Some
Congenital hereditary endothelial dystrophy type 2 (disorder) Is a True Congenital hereditary endothelial dystrophy (disorder) Inferred relationship Some
Corneal dystrophy-perceptive deafness (CDPD) or Harboyan syndrome is a degenerative corneal disorder characterized by the association of congenital hereditary endothelial dystrophy with progressive, postlingual sensorineural hearing loss. Is a True Congenital hereditary endothelial dystrophy (disorder) Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

GB English

US English

Back to Start