Z82.0
BillableFamily history of epilepsy and oth dis of the nervous sys
Family history of epilepsy and other diseases of the nervous system
Coding Notes
Code Also
A second code may be required; sequencing depends on circumstances
Related Codes(8)
Z82.1Family history of blindness and visual loss
Z82.2Family history of deafness and hearing loss
Z82.3Family history of stroke
Z82.4Family hx of ischem heart dis and oth dis of the circ sys
Z82.5Family history of asthma and oth chronic lower resp diseases
Z82.6Family hx of arthrit and oth dis of the ms sys and conn tiss
Z82.7Fam hx of congen malform, deformations and chromsoml abnlt
Z82.8Family hx of disabil and chr dis leading to disablement, NEC
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(140)
SNOMED CT
- Family history of neoplasm of skin160288009
- FH: Huntington's chorea160336000
- Family history of Huntington's chorea160336000
- Family history: Huntington chorea160336000
- Family history: Huntington's chorea160336000
- FH: Disseminated sclerosis160337009
- FH: Multiple sclerosis160337009
- Family history of multiple sclerosis160337009
- Family history: Multiple sclerosis160337009
- FH: Hemiplegia160338004
- Family history: Hemiplegia160338004
- FH: Paraplegia160339007
- Family history: Paraplegia160339007
- FH: Cerebral palsy160340009
- Family history: Cerebral palsy160340009
- FH: Epilepsy160341008
- Family history of epilepsy160341008
- Family history: Epilepsy160341008
- FH: Migraine160342001
- Family history of migraine160342001
- Family history: Migraine160342001
- FH: Muscular dystrophy160343006
- Family history of muscular dystrophy160343006
- Family history: Muscular dystrophy160343006
- FH: Motor neurone disease160344000
- Family history of motor neurone disease160344000
- Family history: Motor neurone disease160344000
- FH: TIA160363004
- Family history of transient ischaemic attack160363004
- Family history of transient ischemic attack160363004
- Family history of acute medical disorder160953001
- Relative - acute medical disorder160953001
- FH: CNS disorder266891008
- Family history of central nervous system disorder266891008
- Family history: CNS disorder266891008
- FH: Parkinsonism275117004
- Family history: Parkinsonism275117004
- FH: Brain disorder275940001
- Family history: Brain disorder275940001
- FH: Nervous system disorder297239000
- Family history of neurological disorder297239000
- Family history: nervous system disorder297239000
- Family history of Parkinson disease297240003
- Family history of Parkinson's disease297240003
- Family history of neoplasm of central nervous system395089003
- Family history of tuberous sclerosis417001009
- Family history of dementia429961000
- Family history of headache disorder429963002
- Family history of Charcot-Marie-Tooth disease429970002
- Family history of sleep apnea430337004
- Family history of sleep apnoea430337004
- Family history of restless legs syndrome430565001
- Family history of seizure disorder430711004
- Family history of amyotrophic lateral sclerosis430727006
- Family history of periodic limb movement disorder430807004
- Family history of movement disorder430809001
- Family history of neuropathy430814002
- Family history of disorder of peripheral nervous system431882002
- Family history of peripheral neuropathy431882002
- Family history of trigeminal neuralgia433496008
- Family history of Steinert myotonic dystrophy63931000119106
- Family history of myotonic muscular dystrophy63931000119106
- Family history of ataxia456651000124101
- Family history of disorder of skeletal and/or smooth muscle456781000124103
- Family history of myopathy456781000124103
- Family history of familial dysautonomia94691000119101
- Family history of narcolepsy16520001000004100
- Family history of spinocerebellar ataxia63881000119101
UMLS
Clinical Terms
- Family history of myotonic muscular dystrophy
- FH: Nervous system disorder
- Family history of Huntington's chorea
- Family history: Migraine
- Relative - acute medical disorder
- Family history: Motor neurone disease
- FH: Paraplegia
- FH: Multiple sclerosis
- Family history of neuropathy
- FH: Huntington's chorea
- Family history of narcolepsy
- Family history of central nervous system disorder
- FH: Hemiplegia
- FH: Migraine
- Family history of migraine
- Family history of restless legs syndrome
- Family history: Huntington chorea
- Family history of transient ischaemic attack
- Family history: Muscular dystrophy
- Family history of neoplasm of skin
- FH: Cerebral palsy
- Family history of Charcot-Marie-Tooth disease
- Family history of Parkinson's disease
- Family history: Huntington's chorea
- Family history: nervous system disorder
- Family history: Cerebral palsy
- Family history of sleep apnoea
- Family history of acute medical disorder
- Family history of transient ischemic attack
- Family history: CNS disorder
- Family history of Steinert myotonic dystrophy
- Family history of peripheral neuropathy
- FH: Parkinsonism
- FH: Epilepsy
- Family history of Parkinson disease
- Family history of ataxia
- Family history of familial dysautonomia
- Conditions classifiable to G00-G99
- Family history of neoplasm of central nervous system
- Family history of headache disorder
- FH: Disseminated sclerosis
- Family history: Hemiplegia
- Family history of muscular dystrophy
- Family history of seizure disorder
- FH: Motor neurone disease
- Family history of movement disorder
- Family history: Paraplegia
- Family history of dementia
- Family history of motor neurone disease
- Family history of neurological disorder
- Family history of tuberous sclerosis
- Family history: Epilepsy
- Family history: Brain disorder
- FH: TIA
- Family history of disorder of skeletal and/or smooth muscle
- Family history of periodic limb movement disorder
- Family history of sleep apnea
- Family history of amyotrophic lateral sclerosis
- Family history of myopathy
- Family history of spinocerebellar ataxia
- FH: CNS disorder
- FH: Muscular dystrophy
- Family history of trigeminal neuralgia
- Family history: Parkinsonism
- Family history of multiple sclerosis
- Family history of epilepsy
- Family history of disorder of peripheral nervous system
- FH: Brain disorder
- Family history: Multiple sclerosis
Frequently Asked Questions
What is the ICD-10 code for family history of epilepsy and oth dis of the nervous sys?
The ICD-10-CM code for family history of epilepsy and oth dis of the nervous sys is Z82.0. The full clinical description is "Family history of epilepsy and other diseases of the nervous system". Z82.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Z82.0 mean?
ICD-10-CM code Z82.0 represents “Family history of epilepsy and other diseases of the nervous system”. It is classified under Chapter 22: Factors Influencing Health Status and Contact With Health Services and is a billable/specific code that can be used on a claim.
Is Z82.0 a billable code?
Yes, Z82.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Z82.0 in?
Z82.0 is in Chapter 22: Factors Influencing Health Status and Contact With Health Services (codes Z00-Z99).
What SNOMED CT codes does Z82.0 map to?
Z82.0 maps to 37 SNOMED CT concepts: 275940001, 266891008, 160340009, 160337009, 160341008, and 32 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Z82.0?
Z82.0 is linked to 2 UMLS Concept Unique Identifiers: C2911226, C0478623. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Z82.0 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like family history of epilepsy and oth dis of the nervous sys affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Z82.0?
Z82.0 maps to the ICD-11 code: QC6Z (Family history of health problems, unspecified).
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.