Autosomal dominant hereditary disorder	Congenital anomaly of intestinal tract	Congenital omphalocele	Developmental hereditary disorder	Digestive system hereditary disorder	Multiple malformation syndrome with facial defects as major feature
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Familial omphalocele syndrome with facial dysmorphism (disorder)
	Familial omphalocele syndrome with facial dysmorphism
	A rare genetic developmental defect during embryogenesis with characteristics of omphalocele associated with facial dysmorphism including flat face, short, upturned nose, long and wide philtrum and flattened maxillary arch and abnormalities of hands.
	familiale omfalocelesyndroom met faciale dysmorfie

Id	770900000
Status	Primitive

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

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

Associated morphology	Hernia
Finding site	Organ within abdominopelvic cavity
Occurrence	Congenital

Associated morphology	Protrusion
Finding site	Intestinal structure
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified