Home > 2006 ICD-9-CM Diagnosis Codes > Supplementary Classification Of Factors Influencing Health Status And Contact With Health Services V01-V85 > Persons With Potential Health Hazards Related To Personal And Family History V10-V19 > Family history of other conditions V19-
2006 ICD-9-CM Diagnosis Code V19.8
Family history of other condition
- Short description: FAMILY HX-CONDITION NEC.
- 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 2006 version of ICD-9-CM V19.8.
- More recent version(s) of ICD-9-CM V19.8: 2007 2008 2009 2010 2011 2012 2013.
V19.8 Alternative Terminology
- Alcoholic offspring
- 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 benign prostatic hyperplasia
- Family history of bulimia nervosa
- Family history of chronic medical disorder
- Family history of clinical finding
- Family history of congestive heart failure
- 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 eating disorder
- Family history of fracture of proximal end of femur
- Family history of headache disorder
- Family history of hereditary disease
- 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 perinatal disorder
- Family history of periodic limb movement disorder
- Family history of physical handicap
- 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 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 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: 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
- 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 V19.8 to ICD-10-CM 
ICD-9-CM V19.8 converts approximately to:
- 2013 ICD-10-CM Z84.89 Family history of other specified conditions
ICD-9-CM Volume 2 Index entries containing back-references to V19.8:
- History (personal) of
family
allergy V19.6
- anemia V18.2
- arteriosclerosis V17.4
- arthritis V17.7
- asthma V17.5
- blindness V19.0
- blood disorder NEC V18.3
- cardiovascular disease V17.4
- carrier, genetic disease V18.9
- cerebrovascular disease V17.1
- chronic respiratory condition NEC V17.6
- congenital anomalies V19.5
- consanguinity V19.7
- coronary artery disease V17.3
- cystic fibrosis V18.1
- deafness V19.2
- diabetes mellitus V18.0
- digestive disorders V18.5
- disease or disorder (of)
allergic V19.6- blood NEC V18.3
- cardiovascular NEC V17.4
- cerebrovascular V17.1
- coronary artery V17.3
- digestive V18.5
- ear NEC V19.3
- endocrine V18.1
- eye NEC V19.1
- genitourinary NEC V18.7
- hypertensive V17.4
- infectious V18.8
- ischemic heart V17.3
- kidney V18.69
- polycystic V18.61
- mental V17.0
- metabolic V18.1
- musculoskeletal NEC V17.89
- osteoporosis V17.81
- neurological NEC V17.2
- parasitic V18.8
- psychiatric condition V17.0
- skin condition V19.4
- ear disorder NEC V19.3
- endocrine disease V18.1
- epilepsy V17.2
- eye disorder NEC V19.1
- genetic disease carrier V18.9
- genitourinary disease NEC V18.7
- glomerulonephritis V18.69
- gout V18.1
- hay fever V17.6
- hearing loss V19.2
- hematopoietic neoplasia V16.7
- Hodgkin's disease V16.7
- Huntington's chorea V17.2
- hydrocephalus V19.5
- hypertension V17.4
- hypospadias V13.61
- infectious disease V18.8
- ischemic heart disease V17.3
- kidney disease V18.69
- polycystic V18.61
- leukemia V16.6
- lymphatic malignant neoplasia NEC V16.7
- malignant neoplasm (of) NEC V16.9
- anorectal V16.0
- anus V16.0
- appendix V16.0
- bladder V16.59
- bone V16.8
- brain V16.8
- breast V16.3
- male V16.8
- bronchus V16.1
- cecum V16.0
- cervix V16.49
- colon V16.0
- duodenum V16.0
- esophagus V16.0
- eye V16.8
- gallbladder V16.0
- gastrointestinal tract V16.0
- genital organs V16.40
- hemopoietic NEC V16.7
- ileum V16.0
- ilium V16.8
- intestine V16.0
- intrathoracic organs NEC V16.2
- kidney V16.51
- larynx V16.2
- liver V16.0
- lung V16.1
- lymphatic NEC V16.7
- ovary V16.41
- oviduct V16.41
- pancreas V16.0
- penis V16.49
- prostate V16.42
- rectum V16.0
- respiratory organs NEC V16.2
- skin V16.8
- specified site NEC V16.8
- stomach V16.0
- testis V16.43
- trachea V16.1
- ureter V16.59
- urethra V16.59
- urinary organs V16.59
- uterus V16.49
- vagina V16.49
- vulva V16.49
- mental retardation V18.4
- metabolic disease NEC V18.1
- mongolism V19.5
- multiple myeloma V16.7
- musculoskeletal disease NEC V17.89
- osteoporosis V17.81
- nephritis V18.69
- nephrosis V18.69
- osteoporosis V17.81
- parasitic disease V18.8
- polycystic kidney disease V18.61
- psychiatric disorder V17.0
- psychosis V17.0
- retardation, mental V18.4
- retinitis pigmentosa V19.1
- schizophrenia V17.0
- skin conditions V19.4
- specified condition NEC V19.8
- stroke (cerebrovascular) V17.1
- visual loss V19.0
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 2006 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.
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