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 certain chronic disabling diseases V17-
2006 ICD-9-CM Diagnosis Code V17.89
Family history of other musculoskeletal diseases
- Short description: FAM HX MUSCULOSK DIS NEC.
- ICD-9-CM V17.89 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 V17.89.
- More recent version(s) of ICD-9-CM V17.89: 2007 2008 2009 2010 2011 2012 2013.
V17.89 Alternative Terminology
- Congenital myasthenia
- Family history of backache
- Family history of juvenile rheumatoid arthritis
- Family history of osteopenia
- Family history of scoliosis deformity of spine
- Family history of synovial cyst of popliteal space
- Family history: ankylosing spondylitis
- Family history: cholinesterase deficiency
- Family history: congenital orthopedic anomaly
- Family history: fragility fracture
- Family history: hip fracture in first degree relative
- Family history: maternal hip fracture
- Family history: maternal hip fracture before age 75
- Family history: muscular dystrophy
- Family history: musculoskeletal disease
- Family history: osteoarthritis
- Maternal history of congenital dislocated hip
Convert V17.89 to ICD-10-CM 
ICD-9-CM V17.89 converts directly to:
- 2013 ICD-10-CM Z82.69 Family history of other diseases of the musculoskeletal system and connective tissue
ICD-9-CM Volume 2 Index entries containing back-references to V17.89:
- 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 V17.89 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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