Auditory system hereditary disorder	Autosomal dominant hereditary disorder	Cardiovascular system hereditary disorder	Congenital conductive hearing loss	Congenital heart disease	Developmental hereditary disorder	Multiple malformation syndrome with facial defects as major feature
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Facial dysmorphism, conductive hearing loss, heart defect syndrome (disorder)
	Facial dysmorphism, conductive hearing loss, heart defect syndrome
	Dysmorphism, conductive hearing loss, heart defect syndrome Tyshchenko syndrome
	A rare multiple congenital anomalies syndrome with characteristics of distinctive facial appearance (low frontal hairline, bilateral ptosis, prominent eyes, flat midface, broad, ﬂat nares, Cupid's bow upper lip vermilion and small, low-set, posteriorly rotated ears), cleft palate, conductive hearing loss, heart defects (atrial or ventricular septal defect) and mild developmental delay/intellectual disability.
	syndroom van faciale dysmorfie, conductief gehoorverlies en hartdefect
	syndroom van dysmorfie, conductief gehoorverlies en hartdefect syndroom van faciale dysmorfie, geleidingsgehoorverlies en hartdefect

Id	763279007
Status	Primitive

Has interpretation	Decreased
Interprets	Hearing

Associated morphology	Morphologically abnormal structure
Finding site	Heart 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	Morphologically abnormal structure
Finding site	Ear 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