2006 ICD-9-CM Diagnosis Code 751.62
Congenital cystic disease of liver
- Short description: CONG CYSTIC LIVER DIS.
- ICD-9-CM 751.62 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 751.62 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 2006 version of ICD-9-CM 751.62.
- More recent version(s) of ICD-9-CM 751.62: 2007 2008 2009 2010 2011 2012 2013 2014 2015.
Convert to ICD-10-CM:
751.62 converts directly to:
- 2015/16 ICD-10-CM Q44.6 Cystic disease of liver
Approximate Synonyms
- Congenital cystic liver
- Cystic liver, congenital
Applies To
- Congenital polycystic disease of liver
- Fibrocystic disease of liver
ICD-9-CM Volume 2 Index entries containing back-references to
751.62:
- Cyst (mucus) (retention) (serous) (simple)
- liver 573.8
- congenital 751.62
- hydatid (see also Echinococcus) 122.8
- Cystic - see also condition
- disease
- liver, congenital 751.62
- Degeneration, degenerative
- Disease, diseased - see also Syndrome
- cystic
- breast (chronic) 610.1
- kidney, congenital (see also Cystic, disease, kidney) 753.10
- liver, congenital 751.62
- lung 518.89
- pancreas 577.2
- renal, congenital (see also Cystic, disease, kidney) 753.10
- semilunar cartilage 717.5
- liver 573.9
- alcoholic 571.3
- chronic 571.9
- cystic, congenital 751.62
- drug-induced 573.3
- due to
- fibrocystic (congenital) 751.62
- glycogen storage 271.0
- organic 573.9
- polycystic (congenital) 751.62
- polycystic (congenital) 759.89
- Fibrocystic
- Polycystic (congenital) (disease) 759.89
- liver 751.62