Anomaly of eye
familiaire primaire hypomagnesiëmie met hypercalciurie en nefrocalcinose
hereditaire aandoening van visueel systeem
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familiaire hypomagnesiëmie met hypercalciurie en nefrocalcinose met ernstige oculaire betrokkenheid (aandoening)
familiaire hypomagnesiëmie met hypercalciurie en nefrocalcinose met ernstige oculaire betrokkenheid
FHHNC met ernstige oculaire betrokkenheid
familiaire hypomagnesiëmie met hypercalciurie en nefrocalcinos met ernstige aantasting van oog
Familial hypomagnesemia hypercalciuria nephrocalcinosis with severe ocular involvement
Id717787005
StatusPrimitive
Associated morphologymorfologische afwijking
Finding sitestructuur van bulbus oculi
Associated morphologypathologische calcificatie
Finding sitenierparenchym
Has interpretationboven referentiebereik
Interpretsbepalen van calcium in urine
SNOMED CT to Orphanet simple map
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetE83.4
TermStoornissen van magnesiummetabolisme
SNOMED CT to ICD-10 extended map
TargetE83.4
RuleTRUE
AdviceALWAYS E83.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
TargetE83.5
RuleTRUE
AdviceALWAYS E83.5
CorrelationSNOMED CT source code to target map code correlation not specified
TargetN29.8
RuleTRUE
AdviceALWAYS N29.8 | THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE
CorrelationSNOMED CT source code to target map code correlation not specified