amelogenesis imperfecta	autosomaal recessieve hereditaire aandoening	hereditaire nefropathie	nefrocalcinose	nierfalen
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amelogenesis imperfecta met nefrocalcinose (aandoening)
	amelogenesis imperfecta met nefrocalcinose
	enamel-renal syndrome amelogenesis imperfecta type IG
	Enamel-renal syndrome
	Amelogenesis imperfecta and nephrocalcinosis Enamel renal syndrome McGibbon Lubinsky syndrome Amelogenesis imperfecta, nephrocalcinosis and impaired renal concentration

Id	109477002
Status	Primitive

Associated morphology	morfologische afwijking
Finding site	structuur van enamelum
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	pathologische calcificatie
Finding site	nierparenchym

Has interpretation	gestoord
Interprets	nierfunctie

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	K00.5
Term	Erfelijke afwijkingen van tandstructuur, niet elders geclassificeerd

Target	E83.5
Term	Stoornissen van calciummetabolisme

Target	N29.8*
Term	Overige aandoeningen van nier en ureter bij elders geclassificeerde overige ziekten

SNOMED CT to Orphanet simple map

1031

SNOMED CT to ICD-10 extended map

Target	K00.5
Rule	TRUE
Advice	ALWAYS K00.5
Correlation	SNOMED CT source code to target map code correlation not specified

Target	E83.5
Rule	TRUE
Advice	ALWAYS E83.5
Correlation	SNOMED CT source code to target map code correlation not specified

Target	N29.8
Rule	TRUE
Advice	ALWAYS N29.8 \| THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE
Correlation	SNOMED CT source code to target map code correlation not specified