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Autosomal recessive agammaglobulinemia due to folliculin interacting protein 1 deficiency (disorder)
Autosomal recessive agammaglobulinemia due to FNIP1 deficiency
Autosomal recessive agammaglobulinemia due to folliculin interacting protein 1 deficiency
Agammaglobulinemia due to FNIP1 defect
Id1351648007
StatusPrimitive
OccurrenceCongenital
Pathological processAbnormal immune process
Finding siteHeart structure
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