Auditory system hereditary disorder	Autosomal recessive hereditary disorder	Congenital disorder of intestine	Congenital neurological disorder	Congenital sensorineural hearing loss	Digestive system hereditary disorder	Disorder of ear	Disorder of gastrointestinal tract	Disorder of sensory function	Hearing loss associated with syndrome	Hereditary sensory neuropathy	Peripheral sensory neuropathy
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Deafness, small bowel diverticulosis, neuropathy syndrome (disorder)
	Deafness, small bowel diverticulosis, neuropathy syndrome
	Groll Hirschowitz syndrome
	Syndrome with characteristics of progressive sensorineural deafness, progressive sensory neuropathy and gastrointestinal abnormalities (progressive loss of gastric motility, small bowel diverticulosis). It has been described in five patients (three sisters in a family and two sisters born to consanguineous parents). This syndrome is transmitted as an autosomal recessive trait.
	syndroom van doofheid, diverticulose van dunne darm en neuropathie

Id	733071009
Status	Primitive

Interprets

Finding site	Ear structure
Occurrence	Congenital

Finding site	Peripheral nerve structure
Occurrence	Congenital

Finding site	Gastrointestinal tract structure
Occurrence	Congenital

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	H90.5
Rule	TRUE
Advice	ALWAYS H90.5 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	G60.8
Rule	TRUE
Advice	ALWAYS G60.8
Correlation	SNOMED CT source code to target map code correlation not specified