Autosomal dominant hereditary disorder	Developmental hereditary disorder	Digestive system hereditary disorder	Hirschsprung's disease	Inherited autonomic nervous system disorder	Intellectual disability
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Mowat-Wilson syndrome (disorder)
	Mowat-Wilson syndrome
	Hirschsprung disease-mental retardation syndrome Hirschsprung disease-intellectual disability syndrome
	Mowat-Wilson-syndroom
	syndroom van ziekte van Hirschsprung en verstandelijke beperking syndroom van Mowat-Wilson syndroom van ziekte van Hirschsprung en mentale retardatie syndroom van ziekte van Hirschsprung en verstandelijke handicap

Id	703535000
Status	Primitive

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

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

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

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

DHD Diagnosis thesaurus reference set

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

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Mowat-Wilson syndrome due to monosomy 2q22