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syndroom van chronische diarree met villusatrofie (aandoening)
syndroom van chronische diarree met villusatrofie
Chronic diarrhea with villous atrophy syndrome
A rare genetic gastroenterological disease characterized by the early onset of chronic diarrhea, vomiting, anorexia, lactic acidosis, renal insufficiency and hepatic involvement (mild elevation of liver enzymes, steatosis, hepatomegaly). Partial villous atrophy (with eosinophilic infiltration) is observed on intestinal biopsy. Although diarrhea may resolve, the development of neurologic symptoms (cerebellar ataxia, sensorineural deafness, seizures), retinitis pigmentosa and muscle weakness may complicate disease course and lead to death. There have been no further descriptions in the literature since 1994.
Id734019006
StatusPrimitive
Clinical coursechronisch
Associated morphologyhyperplasie
Finding sitestructuur van villus intestinalis
Occurrencecongenitaal
Has interpretationgewijzigd
Interpretsdefecatiepatroon
referentieset met complexe 'mapping' naar ICD-10
TargetK59.1
RuleTRUE
AdviceALWAYS K59.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
TargetK63.8
RuleTRUE
AdviceALWAYS K63.8
CorrelationSNOMED CT source code to target map code correlation not specified