Auditory system hereditary disorder	Autosomal dominant hereditary disorder	Congenital hearing disorder	Congenital hearing loss	Developmental hereditary disorder	Disorder of ear	Hearing loss associated with syndrome	Hereditary disorder of musculoskeletal system	Hypertelorism	Multiple system malformation syndrome	Preauricular fistula
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Hypertelorism, preauricular sinus, punctual pits, deafness syndrome (disorder)
	Hypertelorism, preauricular sinus, punctual pits, deafness syndrome
	HPPD (hypertelorism, preauricular sinus, punctual pits, deafness) syndrome Hypertelorism, preauricular sinus, punctual pits, hearing loss syndrome
	A rare developmental defect during embryogenesis syndrome with characteristics of hypertelorism, bilateral preauricular sinus, bilateral punctal pits, lacrimal duct obstruction, hearing loss, abnormal palmar flexion creases and bilateral distal axial triradii. Shawl scrotum has also been reported.
	syndroom van hypertelorisme, pre-auriculaire sinus, punctale fistels en doofheid
	HPPD syndroom van hypertelorisme, pre-auriculaire fistel, punctale fistels en doofheid

Id	773667003
Status	Primitive

Associated morphology	Preauricular sinus
Finding site	Preauricular region structure
Occurrence	Congenital
Pathological process	Pathological developmental process

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

Finding site	Ear structure
Occurrence	Congenital

Interprets

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