gastro-intestinale complicatie	Mowat-Wilson-syndroom
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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
	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) Hirschsprung disease and intellectual disability due to 2q22 microdeletion Hirschsprung disease and intellectual disability due to monosomy 2q22

Id	890118006
Status	Primitive

Associated morphology	dilatatie
Finding site	gedeelte van dikke darm
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	morfologische afwijking
Finding site	structuur van autonome zenuw
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	hypertrofie
Finding site	gedeelte van dikke darm
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Due to

deletie van gedeelte van lange arm van chromosoom 2

Associated morphology	morfologische afwijking
Finding site	structuur van perifeer gedeelte van autonoom zenuwstelsel
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Has interpretation	gestoord
Interprets	intellectueel vermogen

Has interpretation	gestoord
Interprets	Adaptation behavior

SNOMED CT to ICD-10 extended map

Target	Q43.1
Rule	TRUE
Advice	ALWAYS Q43.1
Correlation	SNOMED CT source code to target map code correlation not specified