Autosomal recessive hereditary disorder	Congenital anomaly of abdomen	Congenital diaphragmatic hernia	Congenital hypoplasia of lung	Developmental hereditary disorder	Hereditary disorder of musculoskeletal system	Hereditary myopathy	Multiple malformation syndrome with facial-limb defects as major feature
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Diaphragmatic hernia, abnormal face and distal limb anomalies (disorder)
	Fryns syndrome
	Diaphragmatic hernia, abnormal face and distal limb anomalies
	syndroom van hernia diaphragmatica, afwijkend aangezicht en distale extremiteitafwijkingen
	syndroom van middenrifbreuk, abnormaal aangezicht en anomalieën van vingers en tenen Fryns-syndroom FS syndroom van Fryns

Id	702432006
Status	Primitive

Associated morphology	Hernia
Finding site	Abdomen
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	Hypoplasia
Finding site	Lung structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Hypoplasia
Finding site	Limb structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Hernial opening
Finding site	Diaphragm 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
Correlation	SNOMED CT source code to target map code correlation not specified