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417651000: Congenital hereditary endothelial dystrophy (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
2549868019 Congenital hereditary endothelial dystrophy en Synonym Active Case insensitive SNOMED CT core
2554123017 CHED-congenital hereditary endothelial dystrophy en Synonym Active Case sensitive SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Corneal dystrophy and perceptive deafness syndrome Is a True Congenital hereditary endothelial dystrophy Inferred relationship Some
Congenital hereditary endothelial dystrophy type 1 Is a True Congenital hereditary endothelial dystrophy Inferred relationship Some
Congenital hereditary endothelial dystrophy type 2 Is a True Congenital hereditary endothelial dystrophy Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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