complementdeficiëntie
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immunodeficiëntie door deficiëntie van 'mannan binding lectin serine peptidase 2' (aandoening)
immunodeficiëntie door deficiëntie van 'mannan binding lectin serine peptidase 2'
immunodeficiëntie door MASP2-deficiëntie
Immunodeficiency due to MASP-2 deficiency
Immunodeficiency due to mannan binding lectin serine peptidase 2 deficiency
Immunodeficiency due to MASP-2 (mannan binding lectin serine peptidase 2) deficiency
Immunodeficiency due to MASP-2 deficiency is a rare, genetic immunodeficiency due to a complement cascade protein anomaly characterized by low serum levels of MASP-2 and a variable susceptibility to bacterial infections (e.g. pulmonary tuberculosis, pneumococcal pneumonia, skin abscesses and sepsis), and autoimmune diseases (e.g. inflammatory lung disease, cystic fibrosis, systemic lupus erythematosus). In many cases it remains asymptomatic.
Id771078002
StatusPrimitive
Pathological processafwijkend immuunproces
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetD84.1
TermStoornissen in complementsysteem
SNOMED CT to Orphanet simple map331187
SNOMED CT to ICD-10 extended map
TargetD84.1
RuleTRUE
AdviceALWAYS D84.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified