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Z83
Family history of other specific disorders
ICD10CM code
Medical Policies and Guidelines for Family history of other specific disorders
Related policies from health plans
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Similar Codes
ICD10CM codes
Z83
- Family history of other specific disorders
Z84
- Family history of other conditions
Z84.8
- Family history of other specified conditions
Z84.89
- Family history of other specified conditions
Z86
- Personal history of certain other diseases
Z87
- Personal history of other diseases and conditions
Z83.1
- Family history of other infectious and parasitic diseases
Z81
- Family history of mental and behavioral disorders
Z87.8
- Personal history of other specified conditions
Z83.6
- Family history of other diseases of the respiratory system
HCPCS codes
G8959
- Clinician treating major depressive disorder communicates to clinician treating comorbid condition
G8947
- One or more neuropsychiatric symptoms
G8972
- One or more high risk factors for thromboembolism or more than one moderate risk factor for thromboe
G8370
- Asthma patients with numeric frequency of symptoms or patient completion of an asthma assessment too
G8960
- Clinician treating major depressive disorder did not communicate to clinician treating comorbid cond
D9450
- CASE PRESENTATION
G9012
- Other specified case management service not elsewhere classified
G8992
- Other physical or occupational therapy primary functional limitation, discharge status, at discharge
G8993
- Other physical or occupational therapy subsequent functional limitation, current status, at therapy
G9931
- Documentation of cha2ds2-vasc risk score of 0 or 1
CPT4 codes
81412
- Ashkenazi Jewish associated disorders (eg, Bloom syndrome, Canavan disease, cystic fibrosis, familia
81425
- Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
81410
- Aortic dysfunction or dilation (eg, Marfan syndrome, Loeys Dietz syndrome, Ehler Danlos syndrome typ
81470
- X-linked intellectual disability (XLID) (eg, syndromic and non-syndromic XLID); genomic sequence ana
81416
- Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis, each co
81414
- Cardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT syndrome, catecholamin
81411
- Aortic dysfunction or dilation (eg, Marfan syndrome, Loeys Dietz syndrome, Ehler Danlos syndrome typ
88289
- Chromosome analysis; additional high resolution study
81413
- Cardiac ion channelopathies (eg, Brugada syndrome, long QT syndrome, short QT syndrome, catecholamin
89240
- Unlisted miscellaneous pathology test