Specific code 2010 ICD-9-CM Diagnosis Code V18.19
Family history of other endocrine and metabolic diseases
  • Short description: Fm hx endo/metab dis NEC.
  • ICD-9-CM V18.19 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, V18.19 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
  • You are viewing the 2010 version of ICD-9-CM V18.19.
  • More recent version(s) of ICD-9-CM V18.19: 2011 2012 2013 2014 2015.
Convert to ICD-10-CM: V18.19 converts directly to:
  • 2015/16 ICD-10-CM Z83.49 Family history of other endocrine, nutritional and metabolic diseases
Approximate Synonyms
  • Familial idiopathic hypercalciuria
  • 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 disorder of pancreas
  • 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 hypercholesterolemia in first degree relative
  • Family history of hyperlipoproteinemia (a) (cholesterol problem)
  • Family history of hyperlipoproteinemia A
  • Family history of hyperthyroidism
  • 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 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 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)
  • Family history of xanthelasma
  • Family history of xanthelasma (benign skin deposit)
  • Family history: Cystic fibrosis
  • Family history: Endocrine disorders
  • Family history: Gout
  • Family history: Hypercholesterolemia
  • Family history: Hypothyroidism
  • Family history: Metabolic disorder
  • Family history: Polycystic ovaries
  • Family history: Porphyria
  • Family history: Raised blood lipids
  • Family history: Thyroid disorder
  • Family history: Triglyceride high
  • FH: Cystic fibrosis
  • FH: Endocrine disorders
  • FH: Hypercholesterolemia
  • FH: Metabolic disorder
  • Fhx of compound dyslipidemia
  • Fhx of cystic fibrosis
  • Fhx of endocrine disease
  • Fhx of eruptive xanthoma
  • Fhx of familial combined hyperlipidemia
  • Fhx of familial hyperbetalipoproteinemia
  • Fhx of familial hypercholesterolemia
  • Fhx of familial hypertriglyceridemia
  • Fhx of familial hypoalphalipoproteinemia
  • Fhx of galactosemia
  • Fhx of glycogen storage disease
  • Fhx of hashimotos
  • Fhx of hemochromatosis
  • Fhx of hypercholesterolemia
  • Fhx of hyperlipoproteinemia (a)
  • Fhx of hypobetalipoproteinemia
  • Fhx of lysosomal storage disease
  • Fhx of metabolic disorder
  • Fhx of methylmalonic acidemia
  • Fhx of mitochondrial defect
  • Fhx of phenylketonuria
  • Fhx of propionic acidemia
  • Fhx of tendon xanthoma
  • Fhx of tuberous xanthoma
  • Fhx of urea cycle defect
  • Fhx of xanthelasma
  • Intercritical gout
ICD-9-CM Volume 2 Index entries containing back-references to V18.19:
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM V18.19 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2010 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.