Z82.0

Applicable To

• Conditions classifiable to

Approximate Synonyms

• Family history of alzheimers

• Family history of charcot-marie-tooth disease

• Family history of charcot-marie-tooth disease inherited nerve disease)

• Family history of epilepsy

• Family history of familial dysautonomia

• Family history of familial dysautonomia malfunction of part of nervous system)

• Family history of huntington’s disease inherited brain degenerative disease)

• Family history of migraine

• Family history of muscular dystrophy

• Family history of musculoskeletal dystrophies

• Family history of musculoskeletal dystrophy

• Family history of myotonic muscular dystrophy

• Family history of neurofibromatosis inherited tendency to form nerve tumors)

• Family history of neurological developmental delay

• Family history of neurological disease

• Family history of neurological disorder

• Family history of seizure disorder

• Family history of seizures

• Family history of spinocerebellar ataxia

• Family history of spinocerebellar ataxia inherited brain degenerative disease)

• Family history of steinert myotonic dystrophy

• Family history: neurofibromatosis

• Fh: alzheimer’s disease

• Fh: epilepsy

• Fh: huntington’s chorea

• Fh: migraine

• Fh: muscular dystrophy

• Fhx of alzheimers disease

• Fhx of muscular dystrophy, myotonic

Present On Admission

• Z82.0

Details

• Z82.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• Short description: Family history of epilepsy and oth dis of the nervous sys

• The 2023 edition of ICD-10-CM Z82.0 became effective on October 1, 2022.

• This is the American ICD-10-CM version of Z82.0 – other international versions of ICD-10 Z82.0 may differ.