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Autosomal recessive agammaglobulinemia due to solute carrier family 39 member 7 deficiency (disorder)
Autosomal recessive agammaglobulinemia due to SLC39A7 deficiency
Autosomal recessive agammaglobulinemia due to solute carrier family 39 member 7 deficiency
Id1351665003
StatusPrimitive
Occurrencecongenitaal
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD80.0
RuleTRUE
AdviceALWAYS D80.0
CorrelationSNOMED CT source code to target map code correlation not specified