autosomaal recessieve hereditaire aandoening	congenitale ziekte	familiaire polycytemie
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autosomaal recessieve secundaire polycytemie niet door Von Hippel-Lindau-gen (aandoening)
	autosomaal recessieve secundaire polycytemie niet door Von Hippel-Lindau-gen
	niet-VHL-gen-gerelateerde autosomaal recessieve secundaire polycytemie autosomaal recessieve secundaire erytrocytose niet door Von Hippel-Lindau-gen autosomaal recessieve secundaire polycytemie niet door VHL-gen
	Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene
	Autosomal recessive secondary erythrocytosis non-Chuvash type Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene Autosomal recessive secondary polycythemia non-Chuvash type
	A rare hereditary hematologic disease characterized by an increase in hemoglobin, hematocrit and erythrocyte mass resulting in plethora or ruddy complexion, headache, dizziness, tinnitus and exertional dyspnea. In some cases, thrombophlebitis and arthralgia have also been reported.

Id	783766005
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

247378

SNOMED CT to ICD-10 extended map

Target	D75.1
Rule	TRUE
Advice	ALWAYS D75.1 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified