autosomaal dominante hereditaire aandoening	congenitale ziekte	hereditaire aandoening van erytrocyt	secundaire polycytemie
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autosomaal dominante secundaire polycytemie (aandoening)
	autosomaal dominante secundaire polycytemie
	autosomaal dominante secundaire erytrocytose
	Autosomal dominant secondary polycythemia
	Autosomal dominant secondary erythrocytosis
	A rare, genetic, hematologic disease characterized by increased levels of serum hemoglobin, hematocrit and erythrocyte mass, associated with elevated or inappropriately normal erythropoietin serum levels, occurring in various members of a family and with autosomal dominant inheritance.

Id	783202008
Status	Primitive

Finding site	erytrocyt
Occurrence	congenitaal

Has interpretation	boven referentiebereik
Interprets	telling van erytrocyten

Interprets

hematologische verrichting

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	D75.1
Term	Secundaire polycytemie

SNOMED CT to Orphanet simple map

247511

SNOMED CT to ICD-10 extended map

Target	D75.1
Rule	TRUE
Advice	ALWAYS D75.1
Correlation	SNOMED CT source code to target map code correlation not specified