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Autosomal recessive combined immunodeficiency due to RELB proto-oncogene, NF-kB subunit mutation (disorder)
Autosomal recessive combined immunodeficiency due to RELB mutation
Autosomal recessive combined immunodeficiency due to RELB deficiency
Autosomal recessive combined immunodeficiency due to RelB mutation
Autosomal recessive combined immunodeficiency due to RELB proto-oncogene, NF-kB subunit mutation
Id1351650004
StatusPrimitive
Pathological processafwijkend immuunproces
SNOMED CT to ICD-10 extended map
TargetD81.8
RuleTRUE
AdviceALWAYS D81.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified