autosomaal recessieve hereditaire aandoening
cataract
hereditaire aandoening van bindweefsel
vitreoretinale degeneratie
zeldzame geïsoleerde myopie
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Prolyl 3-hydroxylase 2 gene related high myopia, cataract, vitreoretinal degeneration (disorder)
P3H2 gene related high myopia, cataract, vitreoretinal degeneration
Prolyl 3-hydroxylase 2 gene related high myopia, cataract, vitreoretinal degeneration
Prolyl 3-hydroxylase 2 gene related-high myopia, cataract, vitreoretinal degeneration
LEPREL1 gene related high myopia, cataract, vitreoretinal degeneration
Id1381540004
StatusPrimitive
Associated morphologytroebeling
Finding sitestructuur van lens cristallina
Associated morphologyatrophia
Finding sitestructuur van perifere retina
Associated morphologyatrophia
Finding sitestructuur van corpus vitreum
SNOMED CT to ICD-10 extended map
TargetH44.2
RuleTRUE
AdviceALWAYS H44.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified