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hereditaire viscerale myopathie (aandoening)
hereditaire viscerale myopathie
familiale viscerale myopathie
erfelijke viscerale myopathie
Hereditary hollow viscus myopathy
Familial visceral myopathy
A rare hereditary myopathic degeneration of both gastrointestinal and urinary tracts that causes chronic intestinal pseudo-obstruction. It usually presents after the first decade of life with megaduodenum, megacystis and symptoms such as abdominal distension and/or pain, vomiting, constipation, diarrhea, dysphagia, and/or urinary tract infections.
Id63684002
StatusPrimitive
Associated morphologypseudo-obstructie
Finding sitestructuur van intestinum
Clinical coursechronisch
referentieset met complexe 'mapping' naar ICD-10
TargetG71.8
RuleTRUE
AdviceALWAYS G71.8
CorrelationSNOMED CT source code to target map code correlation not specified