Autosomal dominant hereditary disorder	Congenital anomaly of face bones	Congenital facial dysplasia	Developmental hereditary disorder	Dysostosis	Hereditary disorder of musculoskeletal system	Lesion of face	Multiple malformation syndrome with facial-limb defects as major feature
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Patterson Stevenson Fontaine syndrome (disorder)
	Patterson Stevenson Fontaine syndrome
	Split foot deformity with mandibulofacial dysostosis syndrome
	A very rare variant of acrofacial dysostosis with characteristics of mandibulofacial dysostosis and limb anomalies. It has been described in less than ten patients. The mandibulofacial dysostosis consists of retrognathism, complete or occult posterior cleft palate and anomalies of the external ears. Limb anomalies consist of split-foot deformity with syndactyly of some toes. The condition is transmitted as an autosomal dominant trait with variable penetrance and expressivity.
	syndroom van gespleten voet en mandibulofaciale dysostose
	syndroom van Patterson-Stevenson-Fontaine

Id	724069009
Status	Primitive

Associated morphology	Dysplasia
Finding site	Bone structure of face
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Dysplasia
Finding site	Bone structure of extremity
Occurrence	Congenital
Pathological process	Pathological developmental process

DHD Diagnosis thesaurus reference set

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