autosomaal dominante hereditaire aandoening
cataract
hereditaire aandoening van visueel systeem
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syndroom van hyperferritinemie en congenitaal cataract (aandoening)
syndroom van hyperferritinemie en congenitaal cataract
HHCS
hereditair hyperferritinemie-cataractsyndroom
Hyperferritinemia cataract syndrome
Bonneau-Beaumont syndrome
Hereditary hyperferritinemia-cataract syndrome
Id702398007
StatusDefined
Associated withverhoogd serumferritine
Associated morphologytroebeling
Finding sitestructuur van lens cristallina
DHD Diagnosis thesaurus reference set
SNOMED CT to Orphanet simple map163
SNOMED CT to ICD-10 extended map
TargetH26.0
RuleTRUE
AdviceALWAYS H26.0
CorrelationSNOMED CT source code to target map code correlation not specified