Q44.6
BillableCystic disease of liver
Cystic disease of liver
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Fibrocystic disease of liver
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(7)
Q44.0Agenesis, aplasia and hypoplasia of gallbladder
Q44.1Other congenital malformations of gallbladder
Q44.2Atresia of bile ducts
Q44.3Congenital stenosis and stricture of bile ducts
Q44.4Choledochal cyst
Q44.5Other congenital malformations of bile ducts
Q44.7Other congenital malformations of liver
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(44)
SNOMED CT
- Congenital cystic disease of liver72925005
- Congenital cystic liver72925005
- Congenital hepatic cyst72925005
- Congenital polycystic disease of liver72925005
- Congenital polycystic liver disease72925005
- Cystic disease of liver72925005
- Fibrocystic disease of liver72925005
- Fibrocystic liver disease72925005
- PLD - Polycystic liver disease72925005
- Polycystic liver disease72925005
- Congenital hepatic fibrosis79607001
- Cyst of liver85057007
- Hepatic cyst85057007
- Liver cyst85057007
- Cystic dilation of intrahepatic duct307133008
- Autosomal dominant polycystic liver disease716196007
- Isolated polycystic liver disease716196007
- Caroli syndrome1237346001
- Polycystic liver disease-3 due to heterozygous mutation of ALG8 alpha-1,3-glucosyltransferase gene1366635006
- Polycystic liver disease-3 due to heterozygous mutation of ALG8 gene1366635006
UMLS
Clinical Terms
- Congenital cystic disease of liver
- Cyst of liver
- Congenital cystic liver
- Polycystic liver disease
- Congenital hepatic cyst
- Liver cyst
- Polycystic liver disease-3 due to heterozygous mutation of ALG8 gene
- Congenital polycystic liver disease
- Hepatic cyst
- Cystic dilation of intrahepatic duct
- Cystic liver disease
- Fibrocystic liver disease
- Autosomal dominant polycystic liver disease
- Congenital polycystic disease of liver
- Isolated polycystic liver disease
- PLD - Polycystic liver disease
- Fibrocystic disease of liver
- Congenital hepatic fibrosis
- Polycystic liver disease-3 due to heterozygous mutation of ALG8 alpha-1,3-glucosyltransferase gene
- Caroli syndrome
Frequently Asked Questions
What is the ICD-10 code for cystic disease of liver?
The ICD-10-CM code for cystic disease of liver is Q44.6. The full clinical description is "Cystic disease of liver". Q44.6 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q44.6 mean?
ICD-10-CM code Q44.6 represents “Cystic disease of liver”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q44.6 a billable code?
Yes, Q44.6 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q44.6 in?
Q44.6 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q44.6 map to?
Q44.6 maps to 7 SNOMED CT concepts: 716196007, 1237346001, 72925005, 79607001, 85057007, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q44.6?
Q44.6 is linked to 1 UMLS Concept Unique Identifier: C4551631. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q44.6 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like cystic disease of liver affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Q44.6?
Q44.6 maps to the ICD-11 code: LB20.00 (Fibropolycystic liver disease).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.