autosomaal dominante hereditaire aandoening
congenitale afwijking van voorste oogkamer
hereditaire aandoening van visueel systeem
hereditaire ontwikkelingsstoornis
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Rieger anomaly (disorder)
Rieger anomaly
Rieger anomaly is a congenital ocular defect caused by anterior segment dysgenesis and is characterized by severe anterior chamber deformity with prominent strands and marked atrophy of the iris stroma, with hole or pseudo-hole formation and corectopia. The term covers the association of these iris and pupil anomalies with the features of Axenfeld anomaly.
Id1416355004
StatusPrimitive
Associated morphologymorfologische afwijking
Finding sitestructuur van voorste oogkamer
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to ICD-10 extended map
TargetQ13.8
RuleTRUE
AdviceALWAYS Q13.8
CorrelationSNOMED CT source code to target map code correlation not specified