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anti-p200-pemfigoïd (aandoening)
anti-p200-pemfigoïd
Anti-p200 pemphigoid
A rare, acquired, subepidermal autoimmune bullous disease characterized by polymorphic cutaneous lesions (blisters, urticarial lesions or scars/milia) associated with immunoglobulin G deposition in the basement membrane zone. Lesions are frequently localized on extremities, trunk, palmoplantar and cephalic areas as well as mucous membranes.
Id1228843008
StatusPrimitive
SNOMED CT to Orphanet simple map454710
SNOMED CT to ICD-10 extended map
TargetL12.8
RuleTRUE
AdviceALWAYS L12.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified