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717286002: Grayson Wilbrandt dystrophy of cornea (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3308959015 Grayson Wilbrandt dystrophy of cornea (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3308960013 Grayson Wilbrandt corneal dystrophy en Synonym Active Entire term case sensitive SNOMED CT core module
3312832011 Grayson Wilbrandt dystrophy of cornea en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Grayson Wilbrandt dystrophy of cornea Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Grayson Wilbrandt dystrophy of cornea Is a Corneal opacity true Inferred relationship Existential restriction modifier
Grayson Wilbrandt dystrophy of cornea Is a Hereditary corneal dystrophy true Inferred relationship Existential restriction modifier
Grayson Wilbrandt dystrophy of cornea Is a Bowman's membrane finding true Inferred relationship Existential restriction modifier
Grayson Wilbrandt dystrophy of cornea Finding site Structure of anterior limiting lamina of cornea true Inferred relationship Existential restriction modifier 2
Grayson Wilbrandt dystrophy of cornea Finding site Structure of anterior limiting lamina of cornea true Inferred relationship Existential restriction modifier 3
Grayson Wilbrandt dystrophy of cornea Associated morphology Abnormally opaque structure true Inferred relationship Existential restriction modifier 2
Grayson Wilbrandt dystrophy of cornea Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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