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corneadystrofie van Grayson-Wilbrandt (aandoening)
corneadystrofie van Grayson-Wilbrandt
Grayson-Wilbrandt-corneadystrofie
Grayson Wilbrandt corneal dystrophy
Grayson Wilbrandt dystrophy of cornea
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.
Id717286002
StatusPrimitive
Associated morphologytroebeling
Finding sitestructuur van membraan van Bowman
Associated morphologydystrofie
Finding sitestructuur van membraan van Bowman
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetH18.5
TermHereditaire corneadystrofie├źn
SNOMED CT to Orphanet simple map293375
SNOMED CT to ICD-10 extended map
TargetH18.5
RuleTRUE
AdviceALWAYS H18.5
CorrelationSNOMED CT source code to target map code correlation not specified