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715339004: Autosomal dominant keratitis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3302274016 Autosomal dominant keratitis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3302275015 Autosomal dominant keratitis en Synonym Active Entire term case insensitive SNOMED CT core module
3302276019 Hereditary keratitis 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
Autosomal dominant keratitis Is a Keratitis true Inferred relationship Existential restriction modifier
Autosomal dominant keratitis Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant keratitis Is a Congenital disease true Inferred relationship Existential restriction modifier
Autosomal dominant keratitis Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Autosomal dominant keratitis Associated morphology Inflammation false Inferred relationship Existential restriction modifier 1
Autosomal dominant keratitis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal dominant keratitis Finding site Corneal structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant keratitis Associated morphology Inflammatory morphology true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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