2012 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 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, V17.2 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
- You are viewing the 2012 version of ICD-9-CM V17.2.
- More recent version(s) of ICD-9-CM V17.2: 2013 2014 2015.
Convert to ICD-10-CM:
V17.2 converts directly to:
- 2015/16 ICD-10-CM Z82.0 Family history of epilepsy and other diseases of the nervous system
Approximate 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: Epilepsy
- 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
ICD-9-CM Volume 2 Index entries containing back-references to
V17.2:
- History (personal) of
family
allergy V19.6
