Disorder of gastrointestinal tract
Genetic disease
Inflammatory bowel disease
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Tripartite motif-containing protein 22-related inflammatory bowel disease (disorder)
TRIM22-related inflammatory bowel disease
Tripartite motif-containing protein 22-related inflammatory bowel disease
TRIM22 (tripartite motif-containing protein 22) related inflammatory bowel disease
A rare genetic gastroenterological disease characterized by infantile or childhood onset of severe gastrointestinal inflammation. Patients present with a variable phenotype including fever, diarrhea, failure to thrive, oral ulcers, fistulating perianal disease, strictures, granulomatous colitis, and recurrent bacterial and viral infections.
Id1300124001
StatusPrimitive
Associated morphologyInflammatory morphology
Finding siteGastrointestinal tract structure
Pathological processDysregulated host response
SNOMED CT to Orphanet simple map
SNOMED CT to ICD-10 extended map
TargetK52.8
RuleTRUE
AdviceALWAYS K52.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified