autosomaal recessief hyperimmunoglobuline M-syndroom
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Autosomal recessive hyperimmunoglobulin M syndrome due to catenin beta like 1deficiency (disorder)
Autosomal recessive hyperimmunoglobulin M syndrome due to CTNNBL1 deficiency
Autosomal recessive hyperimmunoglobulin M syndrome due to catenin beta like 1deficiency
Hyper IgM syndrome due to CTNNBL1
Id1351575008
StatusPrimitive
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD80.5
RuleTRUE
AdviceALWAYS D80.5 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified