2012 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 2012 version of ICD-9-CM V18.19.
- More recent version(s) of ICD-9-CM V18.19: 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
family
allergy V19.6
