
2015 ICD-9-CM Diagnosis Code 751.62
Congenital cystic disease of liver
- 2015
- Billable Thru Sept 30/2015
- Non-Billable On/After Oct 1/2015
- 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).
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
Clinical Information
- A usually asymptomatic hereditary disorder which is often associated with polycystic kidney disease. It is characterized by the presence of fluid-filled biliary cysts throughout the liver
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
end stage NEC 572.8


due to hepatitis - see Hepatitis

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