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
Z83.49
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.