Specific code 2011 ICD-9-CM Diagnosis Code V17.2
Family history of other neurological diseases
  • Short description: Fam hx-neurolog dis NEC.
  • ICD-9-CM V17.2 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • ICD-9-CM V17.2 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
  • You are viewing the 2011 version of ICD-9-CM V17.2.
  • More recent version(s) of ICD-9-CM V17.2: 2012 2013 2014.
Disease Synonyms
  • Benign neonatal familial convulsions
  • Familial Alzheimer's disease of late onset
  • Family history of Alzheimers
  • Family history of amyotrophic lateral sclerosis
  • Family history of anencephaly (fetus with severely underdeveloped brain)
  • Family history of Canavan disease
  • Family history of Canavan disease (inherited enzyme disorder)
  • Family history of Charcot-Marie-Tooth disease
  • Family history of Charcot-Marie-Tooth disease (inherited nerve disease)
  • Family history of disorder of peripheral nervous system
  • Family history of epilepsy
  • Family history of Huntington's disease (inherited brain degenerative disease)
  • Family history of learning disability
  • Family history of migraine
  • Family history of movement disorder
  • Family history of myotonic muscular dystrophy
  • Family history of neurological developmental delay
  • Family history of neurological disease
  • Family history of neurological disorder
  • Family history of neuropathy
  • Family history of Parkinson's disease
  • Family history of Rett syndrome
  • Family history of Rett syndrome (genetic disorder)
  • Family history of seizure disorder
  • Family history of seizures
  • Family history of spinal stenosis
  • Family history of spinocerebellar ataxia
  • Family history of spinocerebellar ataxia (inherited brain degenerative disease)
  • Family history of Steinert myotonic dystrophy
  • Family history of Tay-Sachs disease
  • Family history of Tay-Sachs disease (inherited brain degenerative disease)
  • Family history of tremor
  • Family history of trigeminal neuralgia
  • Family history: Alzheimer's disease
  • Family history: Anencephaly
  • Family history: Brain disorder
  • Family history: CNS disorder
  • Family history: Epilepsy
  • Family history: Hemiplegia
  • Family history: Huntington's chorea
  • Family history: Infantile cerebral palsy
  • Family history: Migraine
  • Family history: Motor neurone disease
  • Family history: Multiple sclerosis
  • Family history: Neoplasm of CNS
  • Family history: Paraplegia
  • Family history: Parkinsonism
  • Family history: Senile dementia
  • FH: Alzheimer's disease
  • FH: Anencephaly
  • FH: Huntington's chorea
  • FH: Migraine
  • FHX of Alzheimers
  • Fhx of anencephaly
  • Fhx of Canavan disease
  • Fhx of Charcot-Marie-Tooth disease
  • FHX of epilepsy
  • Fhx of huntington disease
  • Fhx of learning disability
  • Fhx of migraine
  • FHX of muscular dystrophy, myotonic
  • Fhx of myotonic muscular dystrophy
  • Fhx of neurological developmental delay
  • Fhx of neurological disease
  • Fhx of Rett syndrome
  • Fhx of seizures
  • Fhx of spinocerebellar ataxia
  • Fhx of Tay-Sachs disease
Applies To
  • Epilepsy
  • Huntington's chorea
Convert to ICD-10-CM: V17.2 converts directly to:
  • 2014 ICD-10-CM Z82.0 Family history of epilepsy and other diseases of the nervous system
ICD-9-CM Volume 2 Index entries containing back-references to V17.2:
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM V17.2 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2011 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.