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717286002: corneadystrofie van Grayson-Wilbrandt (aandoening)


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
7537581000146111 Grayson-Wilbrandt-corneadystrofie nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7542531000146114 corneadystrofie van Grayson-Wilbrandt (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7542541000146118 corneadystrofie van Grayson-Wilbrandt nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
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


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

This concept is not in any reference sets

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