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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
autosomaal recessieve secundaire erytrocytose niet door Von Hippel-Lindau-gen
autosomaal recessieve secundaire polycytemie niet door VHL-gen
niet-VHL-gen-gerelateerde autosomaal recessieve secundaire polycytemie
Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene
Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene
Autosomal recessive secondary polycythemia non-Chuvash type
Autosomal recessive secondary erythrocytosis 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.
Id783766005
StatusPrimitive
Finding siteerytrocyt
Occurrencecongenitaal
referentieset met complexe 'mapping' naar ICD-10
TargetD75.1
RuleTRUE
AdviceALWAYS D75.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified