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Autosomal recessive agammaglobulinemia due to immunoglobulin heavy chain mu constant region deficiency (disorder)
Autosomal recessive agammaglobulinemia due to immunoglobulin heavy chain mu constant region deficiency
Autosomal recessive agammaglobulinemia due to IGHM mutation
Id1351675000
StatusPrimitive
Occurrencecongenitaal
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD80.0
RuleTRUE
AdviceALWAYS D80.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified