Specific code 2010 ICD-9-CM Diagnosis Code V19.8
Family history of other condition
  • Short description: Family hx-condition NEC.
  • ICD-9-CM V19.8 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • ICD-9-CM V19.8 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
  • You are viewing the 2010 version of ICD-9-CM V19.8.
  • More recent version(s) of ICD-9-CM V19.8: 2011 2012 2013 2014.
Disease Synonyms
  • Alcoholic offspring
  • At risk for heritable disorder based on family history
  • Family history of acquired immune deficiency syndrome
  • Family history of acute medical disorder
  • Family history of alpha-1-antitrypsin deficiency
  • Family history of amnesia
  • Family history of aneurysm of artery
  • Family history of anorexia nervosa
  • Family history of attention deficit hyperactivity disorder
  • Family history of attention deficit hyperactivity disorder, predominantly inattentive type
  • Family history of autosomal aneuploidy
  • Family history of autosomal aneuploidy (abnormal number of chromosomes)
  • Family history of benign prostatic hyperplasia
  • Family history of BRCA gene mutation
  • Family history of BRCA2 gene mutation
  • Family history of breast cancer 2 gene mutation
  • Family history of breast cancer gene (BRCA) mutation
  • Family history of bulimia nervosa
  • Family history of chromosomal abnormality with the patient or offspring at risk
  • Family history of chromosomal disorder with patient at risk
  • Family history of chronic medical disorder
  • Family history of clinical finding
  • Family history of congestive heart failure
  • Family history of Cowden syndrome
  • Family history of Cowden syndrome (inherited skin disease)
  • Family history of cystic hygroma
  • Family history of cystic hygroma (benign tumor)
  • Family history of death due to natural cause
  • Family history of death of unknown cause
  • Family history of disorder
  • Family history of disorder of lung
  • Family history of drug abuse or dependence
  • Family history of eating disorder
  • Family history of fracture of proximal end of femur
  • Family history of headache disorder
  • Family history of hereditary disease
  • Family history of hereditary disease carrier state
  • Family history of heritable cancer
  • Family history of heritable disorder
  • Family history of heritable disorder with the patient or offspring at risk
  • Family history of heritable malignancy
  • Family history of intellectual disability
  • Family history of malignant hyperthermia (heat stroke)
  • Family history of mastoiditis
  • Family history of M�ni�re disease
  • Family history of neoplasm of brain
  • Family history of neoplasm of upper aerodigestive tract
  • Family history of neurofibromatosis (inherited tendency to form nerve tumors)
  • Family history of of drug abuse or dependence
  • Family history of of other condition
  • Family history of of tobacco abuse or dependence
  • Family history of perinatal (near childbirth) problem
  • Family history of perinatal disorder
  • Family history of periodic limb movement disorder
  • Family history of physical handicap
  • Family history of Prader-Willi syndrome
  • Family history of Prader-Willi syndrome (inherited chromosome disorder)
  • Family history of problem behavior
  • Family history of psoriasis with arthropathy
  • Family history of Raynaud phenomenon
  • Family history of restless legs syndrome
  • Family history of sarcoidosis
  • Family history of short stature
  • Family history of sleep apnea
  • Family history of smoking
  • Family history of speech and language disorder
  • Family history of sudden death
  • Family history of systemic sclerosis
  • Family history of tobacco abuse or dependence
  • Family history of trisomy 13
  • Family history of trisomy 13 (inherited chromosome disorder)
  • Family history of trisomy 18
  • Family history of trisomy 18 (inherited chromosome disorder)
  • Family history of Turner syndrome
  • Family history of Turner syndrome (45, X) (inherited chromosome disorder)
  • Family history of ventricular premature beats
  • Family history: Alopecia
  • Family history: Anxiety state
  • Family history: Autoimmune disease
  • Family history: Breast disease
  • Family history: Death under 60 years
  • Family history: Dyslexia
  • Family history: Early menarche
  • Family history: Early menopause
  • Family history: Female infertility
  • Family history: Hirsutism
  • Family history: Late menarche
  • Family history: Late menopause
  • Family history: Male infertility
  • Family history: Malignant hyperpyrexia
  • Family history: Menstrual disorder
  • Family history: Mental retardation
  • Family history: neurofibromatosis
  • Family history: Nutritional deficiency
  • Family history: Obesity
  • Family history: Obstetric problem
  • Family history: Raised blood pressure in pregnancy
  • Family history: Serious disease
  • Family history: Spina bifida
  • Family history: Sudden infant death
  • FH: Malignant hyperpyrexia
  • FH: Mental retardation
  • Fhx of autosomal aneuploidy
  • Fhx of BRCA gene mutation
  • Fhx of BRCA2 gene mutation
  • Fhx of chromosomal abnormality at risk
  • Fhx of cowden syndrome
  • Fhx of cystic hygroma
  • Fhx of drug abuse or dependence
  • Fhx of heritable cancer
  • Fhx of heritable disorder
  • Fhx of heritable disorder, at risk
  • Fhx of heritable disorder, carrier
  • Fhx of intellectual disability
  • Fhx of malignant hyperthermia
  • Fhx of neurofibromatosis
  • Fhx of other condition
  • Fhx of perinatal problem
  • Fhx of Prader-Willi syndrome
  • Fhx of short stature
  • Fhx of sudden death
  • Fhx of tobacco abuse or dependence
  • Fhx of trisomy 13
  • Fhx of trisomy 18
  • Fhx of Turner syndrome (45,X)
  • Heredofamilial brachial plexus paralysis syndrome
  • History of handicap in child of subject
  • History of stable aneurysm of abdominal aorta
  • Hyperbetalipoproteinemia
  • Maternal history of disorder
  • Maternal injury
  • Maternal medical problem
  • Maternal prolapsed cord
  • Maternal pyrexia
  • Sibling is handicapped
  • Vertical alopecia
Convert to ICD-10-CM: V19.8 converts approximately to:
  • 2014 ICD-10-CM Z84.89 Family history of other specified conditions
ICD-9-CM Volume 2 Index entries containing back-references to V19.8:
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM V19.8 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.