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hereditaire niet-sferocytaire hemolytische anemie door verhoogde activiteit van adenosinedeaminase (aandoening)
hereditaire niet-sferocytaire hemolytische anemie door verhoogde activiteit van adenosinedeaminase
HNSHA door verhoogde ADA-activiteit
erfelijke niet-sferocytaire hemolytische anemie door verhoogde activiteit van adenosinedesaminase
Hemolytic anemia due to erythrocyte adenosine deaminase overproduction
Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity
Adenosine deaminase superactivity
HNSHA (hereditary nonspherocytic hemolytic anemia) due to increased adenosine deaminase activity
A rare genetic hematologic disease characterized by mild chronic hemolytic anemia (due to highly elevated adenosine deaminase activity in red blood cells resulting in their premature destruction), elevated reticulocyte count, splenomegaly and mild hyperbilirubinemia. Other cells and tissues are not affected.
Id5315003
StatusPrimitive
Finding siteerytrocyt
Has interpretationaanwezig
Interpretshemolyse
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetD55.8
TermOverige anemie├źn door gespecificeerde enzymstoornissen
SNOMED CT to Orphanet simple map99138
SNOMED CT to ICD-10 extended map
TargetD55.8
RuleTRUE
AdviceALWAYS D55.8
CorrelationSNOMED CT source code to target map code correlation not specified