2019 ICD-10-CM Diagnosis Code Z83.49

Family history of other endocrine, nutritional and metabolic diseases

    2016 2017 2018 2019 Billable/Specific Code POA Exempt
  • Z83.49 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • Short description: Family history of endo, nutritional and metabolic diseases
  • The 2019 edition of ICD-10-CM Z83.49 became effective on October 1, 2018.
  • This is the American ICD-10-CM version of Z83.49 - other international versions of ICD-10 Z83.49 may differ.
The following code(s) above Z83.49 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to Z83.49:
  • Z00-Z99
    2019 ICD-10-CM Range Z00-Z99

    Factors influencing health status and contact with health services

    Note
    • Z codes represent reasons for encounters. A corresponding procedure code must accompany a Z code if a procedure is performed. Categories Z00-Z99 are provided for occasions when circumstances other than a disease, injury or external cause classifiable to categories A00-Y89 are recorded as 'diagnoses' or 'problems'. This can arise in two main ways:
    • (a) When a person who may or may not be sick encounters the health services for some specific purpose, such as to receive limited care or service for a current condition, to donate an organ or tissue, to receive prophylactic vaccination (immunization), or to discuss a problem which is in itself not a disease or injury.
    • (b) When some circumstance or problem is present which influences the person's health status but is not in itself a current illness or injury.
    Factors influencing health status and contact with health services
  • Z77-Z99
    2019 ICD-10-CM Range Z77-Z99

    Persons with potential health hazards related to family and personal history and certain conditions influencing health status

    Code Also
    • any follow-up examination (Z08-Z09)
    Persons with potential health hazards related to family and personal history and certain conditions influencing health status
  • Z83
    ICD-10-CM Diagnosis Code Z83

    Family history of other specific disorders

      2016 2017 2018 2019 Non-Billable/Non-Specific Code
    Type 2 Excludes
    • contact with and (suspected) exposure to communicable disease in the family (Z20.-)
    Family history of other specific disorders
  • Z83.4
    ICD-10-CM Diagnosis Code Z83.4

    Family history of other endocrine, nutritional and metabolic diseases

      2016 2017 2018 2019 Non-Billable/Non-Specific Code
    Applicable To
    Family history of other endocrine, nutritional and metabolic diseases
Approximate Synonyms
  • Family history of canavan disease
  • Family history of canavan disease (inherited enzyme disorder)
  • Family history of combined hyperlipidemia
  • Family history of compound dyslipidemia
  • Family history of compound dyslipidemia (cholesterol problem)
  • Family history of cystic fibrosis
  • Family history of endocrine disease
  • Family history of eruptive xanthoma
  • Family history of eruptive xanthoma (benign skin deposit)
  • Family history of familial combined hyperlipidemia (cholesterol problem)
  • Family history of familial hyperbetalipoproteinemia (cholesterol problem)
  • Family history of familial hypercholesterolemia (high cholesterol)
  • Family history of familial hypertriglyceridemia
  • Family history of familial hypoalphalipoproteinemia (inherited disorder leads to low hdl level)
  • Family history of galactosemia
  • Family history of galactosemia (inherited enzyme disorder)
  • Family history of glycogen storage disease
  • Family history of hashimoto's (autoimmune cause of low thyroid function)
  • Family history of hashimotos thyroiditis
  • Family history of hemochromatosis
  • Family history of hemochromatosis (iron overload)
  • Family history of hyperbetalipoproteinemia
  • Family history of hypercholesterolemia
  • Family history of hypercholesterolemia (high cholesterol)
  • Family history of hyperlipoproteinemia (a) (cholesterol problem)
  • Family history of hyperlipoproteinemia a
  • Family history of hypertriglyceridemia
  • Family history of hypoalphalipoproteinemia
  • Family history of hypobetalipoproteinemia
  • Family history of hypobetalipoproteinemia (cholesterol problem)
  • Family history of lysosomal storage disease
  • Family history of lysosomal storage disease (inherited disorder of cells)
  • Family history of metabolic disorder
  • Family history of methylmalonic acidemia (inherited enzyme disorder)
  • Family history of methylmalonic aciduria
  • Family history of mitochondrial (structure of cell) defect
  • Family history of mitochondrial defect
  • Family history of mitochondrial disease
  • Family history of of endocrine disease
  • Family history of phenylketonuria (inherited enzyme disorder)
  • Family history of phenylketonuria (pku)
  • Family history of propionic acidemia (inherited enzyme disorder)
  • Family history of propionic aciduria
  • Family history of pseudocholinesterase deficiency
  • Family history of pseudocholinesterase deficiency (inherited enzyme disorder)
  • Family history of tay-sachs disease
  • Family history of tay-sachs disease (inherited brain degenerative disease)
  • Family history of tendon xanthoma
  • Family history of tendon xanthoma (benign deposit in tendon)
  • Family history of tuberous xanthoma
  • Family history of tuberous xanthoma (benign skin deposit)
  • Family history of urea cycle defect
  • Family history of urea cycle defect (inherited enzyme disorder)
  • Fh: cystic fibrosis
  • Fh: endocrine disorders
  • Fh: hypercholesterolemia
  • Fh: metabolic disorder
Present On Admission
POA Help
"Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA.
  • Z83.49 is considered exempt from POA reporting.
ICD-10-CM Z83.49 is grouped within Diagnostic Related Group(s) (MS-DRG v36.0):
  • 795 Normal newborn
  • 951 Other factors influencing health status

Convert Z83.49 to ICD-9-CM

Code History
  • 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
  • 2017 (effective 10/1/2016): No change
  • 2018 (effective 10/1/2017): No change
  • 2019 (effective 10/1/2018): No change

Diagnosis Index entries containing back-references to Z83.49:

ICD-10-CM Codes Adjacent To Z83.49
Z83.0 Family history of human immunodeficiency virus [HIV] disease
Z83.1 Family history of other infectious and parasitic diseases
Z83.2 Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Z83.3 Family history of diabetes mellitus
Z83.4 Family history of other endocrine, nutritional and metabolic diseases
Z83.41 Family history of multiple endocrine neoplasia [MEN] syndrome
Z83.42 Family history of familial hypercholesterolemia
Z83.43 Family history of other disorder of lipoprotein metabolism and other lipidemias
Z83.430 Family history of elevated lipoprotein(a)
Z83.438 Family history of other disorder of lipoprotein metabolism and other lipidemia
Z83.49 Family history of other endocrine, nutritional and metabolic diseases
Z83.5 Family history of eye and ear disorders
Z83.51 Family history of eye disorders
Z83.511 Family history of glaucoma
Z83.518 Family history of other specified eye disorder
Z83.52 Family history of ear disorders
Z83.6 Family history of other diseases of the respiratory system
Z83.7 Family history of diseases of the digestive system
Z83.71 Family history of colonic polyps
Z83.79 Family history of other diseases of the digestive system
Z84 Family history of other conditions

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.