Auditory system hereditary disorder	Autosomal hereditary disorder	Congenital sensorineural hearing loss	Decreased hearing	Developmental hereditary disorder	Dystrophia unguium	Ectodermal dysplasia with nail defect	Genetic disorder of nail	Hearing loss associated with syndrome	Hereditary disorder of the integument	Intellectual disability
\|	\|	\|	\|	\|	\|	\|	\|	\|	\|	\|

Deafness with onychodystrophy syndrome (disorder)
	Deafness with onychodystrophy syndrome
	A group of rare genetic developmental defect during embryogenesis disorders with the association of sensorineural deafness and onychodystrophy (for example absent/hypoplastic finger and toenails) as well as brachydactyly and finger-like thumbs.
	syndroom van doofheid en onychodystrofie
	syndroom van doofheid en dystrophia unguium

Id	773735007
Status	Primitive

Finding site	Structure of auditory system
Occurrence	Congenital

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

Associated morphology	Dysplasia
Finding site	Ectoderm structure
Occurrence	Congenital
Pathological process	Pathological developmental process

Has interpretation	Decreased
Interprets	Hearing

Associated morphology	Dystrophy
Finding site	Nail unit structure
Occurrence	Congenital
Pathological process	Pathological developmental process

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

|

Autosomal dominant deafness with onychodystrophy syndrome