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717286002: Grayson Wilbrandt dystrophy of cornea (disorder)


Status: current, Primitive. 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 Case sensitive SNOMED CT core
3308960013 Grayson Wilbrandt corneal dystrophy en Synonym Active Case sensitive SNOMED CT core
3312832011 Grayson Wilbrandt dystrophy of cornea en Synonym Active Case sensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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