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.
Associated morphologypseudo-obstructie
Finding sitestructuur van intestinum
Clinical coursechronisch
DHD Diagnosis thesaurus reference set
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TermOverige gespecificeerde primaire spieraandoeningen
SNOMED CT to Orphanet simple map2604
SNOMED CT to ICD-10 extended map
AdviceALWAYS G71.8
CorrelationSNOMED CT source code to target map code correlation not specified