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Mowat-Wilson-syndroom door monosomie 2q22 (aandoening)
Mowat-Wilson-syndroom door monosomie 2q22
syndroom van Mowat-Wilson door monosomie van chromosoom 2q22
Mowat-Wilson syndrome due to monosomy 2q22
Hirschsprung disease and intellectual disability due to 2q22 microdeletion
Hirschsprung disease and intellectual disability due to monosomy 2q22
Mowat-Wilson syndrome due to 2q22 microdeletion
Hirschsprung disease and intellectual disability due to del(2)(q22)
Mowat-Wilson syndrome due to del(2)q(22)
Id890118006
StatusPrimitive
Associated morphologydilatatie
Finding sitegedeelte van dikke darm
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
Associated morphologyhypertrofie
Finding sitegedeelte van dikke darm
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetQ43.1
RuleTRUE
AdviceALWAYS Q43.1
CorrelationSNOMED CT source code to target map code correlation not specified