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congenitaal cataract en microcornea met troebeling van cornea (aandoening)
congenitaal cataract en microcornea met troebeling van cornea
congenitaal cataract en microcornea met opaciteit van hoornvlies
Congenital cataract microcornea with corneal opacity
CCMCO - congenital cataract microcornea with corneal opacity
A rare genetic eye disease with characteristics of congenital cataract, microcornea and corneal opacity resulting in severe visual impairment or blindness. Depending on the genetic background, other developmental ocular defects may also be present.
Id1279837000
StatusPrimitive
Associated morphologytroebeling
Finding sitestructuur van lens cristallina
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologyafwijkend klein
Finding sitestructuur van cornea
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologytroebeling
Finding sitestructuur van cornea
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
SNOMED CT to Orphanet simple map289499
SNOMED CT to ICD-10 extended map
TargetQ12.0
RuleTRUE
AdviceALWAYS Q12.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified