FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

416633008: Congenital hereditary endothelial dystrophy type 1 (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
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
258931000052111 medfödd ärftlig endoteldystrofi, dominant form sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start