Gastrointestinal complication	Mowat-Wilson syndrome
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Mowat-Wilson syndrome due to monosomy 2q22 (disorder)
	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
	Mowat-Wilson-syndroom door monosomie 2q22
	syndroom van Mowat-Wilson door monosomie van chromosoom 2q22

Id	890118006
Status	Primitive

Associated morphology	Dilatation
Finding site	Large intestine part
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Morphologically abnormal structure
Finding site	Autonomic nerve structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Hypertrophy
Finding site	Large intestine part
Occurrence	Congenital
Pathological process	Pathological developmental process

Due to

Deletion of part of long arm of chromosome 2

Associated morphology	Morphologically abnormal structure
Finding site	Structure of peripheral part of autonomic nervous system
Occurrence	Congenital
Pathological process	Pathological developmental process

ICD-10 complex map reference set

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