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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
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
3312833018 An extremely rare form of corneal dystrophy with manifestation of variable patterns of opacification in the Bowman layer of the cornea that extend anteriorly into the epithelium with decreased to normal visual acuity. Onset is in the first to second decade of life. Patients develop painful erosions that are less severe than those in Reis-Bucklers corneal dystrophy and Thiel-Behnke corneal dystrophy. Visual acuity is normal or sometimes slightly decreased. The condition has a progressive course. An autosomal dominant pattern of inheritance has been reported. en Definition 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
601171000274113 GWCD - Grayson-Wilbrandt-Hornhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3414561001000112 Grayson-Wilbrandt-Hornhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6295631000241116 dystrophie cornéenne de Grayson-Wilbrandt fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6295631000241116 dystrophie cornéenne de Grayson-Wilbrandt fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
601171000274113 GWCD - Grayson-Wilbrandt-Hornhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3414561001000112 Grayson-Wilbrandt-Hornhautdystrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

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 Existential restriction modifier (core metadata concept)
Grayson Wilbrandt dystrophy of cornea (disorder) Is a Corneal opacity true Inferred relationship Existential restriction modifier (core metadata concept)
Grayson Wilbrandt dystrophy of cornea (disorder) Is a Hereditary corneal dystrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Grayson Wilbrandt dystrophy of cornea (disorder) Is a Bowman's membrane finding true Inferred relationship Existential restriction modifier (core metadata concept)
Grayson Wilbrandt dystrophy of cornea (disorder) Finding site Structure of anterior limiting lamina of cornea (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Grayson Wilbrandt dystrophy of cornea (disorder) Finding site Structure of anterior limiting lamina of cornea (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Grayson Wilbrandt dystrophy of cornea (disorder) Associated morphology Opacity true Inferred relationship Existential restriction modifier (core metadata concept) 2
Grayson Wilbrandt dystrophy of cornea (disorder) Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 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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