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417651000: Congenital hereditary endothelial dystrophy (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2547521014 Congenital hereditary endothelial dystrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2549868019 Congenital hereditary endothelial dystrophy en Synonym Active Entire term case insensitive SNOMED CT core module
2554123017 CHED-congenital hereditary endothelial dystrophy en Synonym Active Entire term case sensitive SNOMED CT core module


3 descendants. Search Descendants:

Expanded Value Set


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

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

This concept is not in any reference sets

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