Congenital absence of spleen	Congenital diaphragmatic hernia	Congenital short bowel syndrome	Genetic disease	Multiple malformation syndrome with facial defects as major feature
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Diaphragmatic hernia, short bowel, asplenia syndrome (disorder)
	Diaphragmatic hernia, short bowel, asplenia syndrome
	A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of congenital diaphragmatic hernia, short bowel, and asplenia. Dysmorphic facial features include long forehead, hypertelorism, upturned nares and small mandible. Atresia of the duodenum has also been reported.

Id	1217373008
Status	Primitive

Associated morphology	Abnormally short growth
Finding site	Entire small intestine
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Hernial opening
Finding site	Diaphragm structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Hernia
Finding site	Abdomen
Occurrence	Congenital

Associated morphology	Absence
Finding site	Splenic structure
Occurrence	Congenital
Pathological process	Pathological developmental process

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

ICD-10 complex map reference set

Target	Q87.0
Rule	TRUE
Advice	ALWAYS Q87.0 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified