autosomaal dominante hereditaire aandoening
ernstige gecombineerde immunodeficiëntie met laag aantal T- en B-cellen
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Autosomal dominant T-cell negative, B-cell negative severe combined immunodeficiency due to activated Rac family small GTPase 2 defect (disorder)
Autosomal dominant T-cell negative, B-cell negative severe combined immunodeficiency due to activated RAC2 defect
Autosomal dominant T-cell negative, B-cell negative severe combined immunodeficiency due to activated Rac family small GTPase 2 defect
Autosomal dominant T-B- SCID (severe combined immunodeficiency) due to activated RAC2 defect
Id1351235001
StatusPrimitive
Occurrencecongenitaal
Finding sitestructuur van immuunsysteem
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD81.1
RuleTRUE
AdviceALWAYS D81.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified