Autosomal recessive hereditary disorder	Choanal atresia	Congenital anomaly of skull	Developmental hereditary disorder	Digestive system hereditary disorder	Hereditary disorder of musculoskeletal system	Multiple malformation syndrome with facial defects as major feature
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Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome (disorder)
	Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome
	Burn McKeown syndrome
	An extremely rare multiple congenital anomaly syndrome with characteristics of bilateral choanal atresia associated with cranio-facial dysmorphism, that can be accompanied by hearing loss, unilateral cleft lip, preauricular tags, cardiac septal defects and anomalies of the kidneys. The features of this syndrome overlap considerably with those of the CHARGE syndrome.
	syndroom van choanale atresie, gehoorverlies, hartdefect en craniofaciale dysmorfie
	syndroom van Burn-McKeown

Id	720640005
Status	Primitive

Associated morphology	Morphologically abnormal structure
Finding site	Bone structure of cranium
Occurrence	Congenital
Pathological process	Pathological developmental process

Associated morphology	Congenital atresia
Finding site	Structure of choana
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