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417395001: Congenital hereditary endothelial dystrophy type 2 (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
2553628017 Congenital hereditary endothelial dystrophy, autosomal recessive form en Synonym Active Entire term case insensitive SNOMED CT core module
3776017011 Congenital hereditary endothelial dystrophy type 2 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3776018018 CHED II - Congenital hereditary endothelial dystrophy II en Synonym Active Entire term case sensitive SNOMED CT core module
3776019014 Congenital hereditary endothelial dystrophy type 2 en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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