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chronische enteropathie door mutatie in 'solute carrier organic anion transporter family member 2A1'-gen (aandoening)
chronische enteropathie door mutatie in SLCO2A1-gen
chronische darmaandoening door SLCO2A1-mutatie
chronische enteropathie door mutatie in 'solute carrier organic anion transporter family member 2A1'-gen
Chronic enteropathy associated with SLCO2A1 gene
Chronic enteropathy associated with solute carrier organic anion transporter family member 2A1 gene
A rare genetic gastroenterological disease characterized by the presence of multiple persistent, intractable ulcers of the small intestine, leading to chronic blood and protein loss. Signs and symptoms include abdominal pain, anemia, fatigue, edema, and diarrhea. Morphologically, the condition manifests with multiple sharply demarcated shallow lesions with irregular circular or linear shape.
Id1187194006
StatusPrimitive
Clinical coursechronisch persisterend
Associated morphologymultipele ulcera
Finding sitestructuur van intestinum tenue
SNOMED CT to Orphanet simple map468641
SNOMED CT to ICD-10 extended map
TargetK63.3
RuleTRUE
AdviceALWAYS K63.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified