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gecombineerde immunodeficiëntie door RELA-haplo-insufficiëntie (aandoening)
gecombineerde immunodeficiëntie door RELA-haplo-insufficiëntie
gecombineerde immuundeficiëntie door haplo-insufficiëntie van RELA-gen
Combined immunodeficiency due to RELA haploinsufficiency
A rare non-severe combined immunodeficiency characterized by tumor necrosis factor-dependent chronic mucocutaneous ulcerations and inflammatory bowel disease presenting during the first years of life. Ulcerations occur primarily in the oral, gastrointestinal, and vaginal mucosa.
Id1336027001
StatusPrimitive
Clinical coursechronisch
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