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717286002: Grayson Wilbrandt dystrophy of cornea (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3308959015 Grayson Wilbrandt dystrophy of cornea (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3308960013 Grayson Wilbrandt corneal dystrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312832011 Grayson Wilbrandt dystrophy of cornea en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401553019 Grayson-Wilbrandt corneal dystrophy (GWCD) is an extremely rare form of corneal dystrophy characterized by variable patterns of opacification in the Bowman layer of the cornea which extend anteriorly into the epithelium with decreased to normal visual acuity. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401554013 Grayson-Wilbrandt corneal dystrophy (GWCD) is an extremely rare form of corneal dystrophy characterised by variable patterns of opacification in the Bowman layer of the cornea which extend anteriorly into the epithelium with decreased to normal visual acuity. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Grayson Wilbrandt dystrophy of cornea (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Grayson Wilbrandt dystrophy of cornea (disorder) Is a Corneal opacity true Inferred relationship Some
Grayson Wilbrandt dystrophy of cornea (disorder) Is a Hereditary corneal dystrophy true Inferred relationship Some
Grayson Wilbrandt dystrophy of cornea (disorder) Is a Bowman's membrane finding true Inferred relationship Some
Grayson Wilbrandt dystrophy of cornea (disorder) Finding site Anterior limiting lamina of cornea true Inferred relationship Some 2
Grayson Wilbrandt dystrophy of cornea (disorder) Finding site Anterior limiting lamina of cornea true Inferred relationship Some 3
Grayson Wilbrandt dystrophy of cornea (disorder) Associated morphology Opacity true Inferred relationship Some 2
Grayson Wilbrandt dystrophy of cornea (disorder) Associated morphology Dystrophy true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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