V19.8 - Family History Of Other Condition
The ICD 9 Code for Family history of other condition is listed as V19.8.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
| ICD 9 CM Field | Value |
|---|---|
| Diagnosis Code: | V19.8 |
| Long Description: | Family history of other condition |
| Short Description: | Family hx-condition NEC |
| Chapter: | Supplementary Classification Of Factors Influencing Health Status And Contact With Health Services |
| Block: | Persons With Potential Health Hazards Related To Personal And Family History (V10-V19) |
| Related Descriptions: |
Alcoholic offspring (situation)
Family history of acquired immune deficiency syndrome (situation) Family history of acute medical disorder (situation) Family history of alcoholism (situation) Family history of alpha-1-antitrypsin deficiency (situation) Family history of amnesia (situation) Family history of aneurysm of artery (situation) Family history of anorexia nervosa (situation) Family history of attention deficit hyperactivity disorder (situation) Family history of attention deficit hyperactivity disorder, predominantly inattentive type (situation) Family history of benign prostatic hyperplasia (situation) Family history of bulimia nervosa (situation) Family history of chronic medical disorder (situation) Family history of clinical finding (situation) Family history of congestive heart failure (situation) Family history of death due to natural cause (situation) Family history of death of unknown cause (situation) Family history of disorder (situation) Family history of disorder of lung (situation) Family history of eating disorder (situation) Family history of edema of lower extremity (situation) Family history of fracture of proximal end of femur (situation) Family history of headache disorder (situation) Family history of hereditary disease (situation) Family history of M Family history of mastoiditis (situation) Family history of mitochondrial disease (situation) Family history of neoplasm of brain (situation) Family history of neoplasm of upper aerodigestive tract (situation) Family history of perinatal disorder (situation) Family history of periodic limb movement disorder (situation) Family history of physical handicap (situation) Family history of problem behavior (situation) Family history of psoriasis with arthropathy (situation) Family history of Raynaud phenomenon (situation) Family history of restless legs syndrome (situation) Family history of sarcoidosis (situation) Family history of sleep apnea (situation) Family history of smoking (situation) Family history of speech and language disorder (situation) Family history of sudden death (situation) Family history of systemic sclerosis (situation) Family history of ventricular premature beats (situation) Family history: Alopecia (situation) Family history: Anxiety state (situation) Family history: Autoimmune disease (situation) Family history: Breast disease (situation) Family history: Death under 60 years (situation) Family history: Dyslexia (situation) Family history: Early menarche (situation) Family history: Early menopause (situation) Family history: Female infertility (situation) Family history: Hirsutism (situation) Family history: Late menarche (situation) Family history: Late menopause (situation) Family history: Male infertility (situation) Family history: Malignant hyperpyrexia (situation) Family history: Menstrual disorder (situation) Family history: Nutritional deficiency (situation) Family history: Obesity (situation) Family history: Obstetric problem (situation) Family history: Raised blood pressure in pregnancy (situation) Family history: Serious disease (situation) Family history: Spina bifida (situation) Family history: Sudden infant death (situation) Heredofamilial brachial plexus paralysis syndrome History of handicap in child of subject (situation) History of stable aneurysm of abdominal aorta (situation) Hyperbetalipoproteinemia Maternal history of disorder (situation) Maternal injury (situation) Maternal medical problem (situation) Maternal prolapsed cord (situation) Maternal pyrexia (situation) Sibling is handicapped (situation) Vertical alopecia |
| ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD-10-CM Code: | Z84.89 - Family history of other specified conditions (approximate) |
| ICD-9-CM Siblings (same level / similar specificity) of V19.8: | |
| V19.0 - Family history of blindness or visual loss | |
| V19.2 - Family history of deafness or hearing loss | |
| V19.3 - Family history of other ear disorders | |
| V19.4 - Family history of skin conditions | |
| V19.5 - Family history of congenital anomalies | |
| V19.6 - Family history of allergic disorders | |
| V19.7 - Family history of consanguinity | |