Z83.49

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

• Z83.49

Details

• 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 2023 edition of ICD-10-CM Z83.49 became effective on October 1, 2022.

• This is the American ICD-10-CM version of Z83.49 – other international versions of ICD-10 Z83.49 may differ.