Auditory system hereditary disorder
Autosomal dominant hereditary disorder
Central nervous system complication
Diabetes mellitus associated with genetic syndrome
Digestive system hereditary disorder
Disorder of brain
Disorder of endocrine pancreas
Hereditary disorder of endocrine system
Hereditary disorder of nervous system
Hereditary metabolic disease
Hereditary nephropathy
Metabolic renal disease
Neural hearing loss
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Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (disorder)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
Herrmann syndrome
syndroom van lichtgevoelige myoklonie, diabetes mellitus, doofheid, nefropathie en hersendisfunctie
Id237612000
StatusPrimitive
Finding siteEndocrine pancreatic structure
Finding siteKidney structure
Finding siteCerebrum
Finding siteVestibulocochlear nerve structure
Finding siteStructure of auditory system
InterpretsHearing
Associated withGenetic disease
ICD-10 complex map reference set
TargetE14.7
RuleTRUE
AdviceALWAYS E14.7
CorrelationSNOMED CT source code to target map code correlation not specified