Q44.79
BillableOther congenital malformations of liver
Other congenital malformations of liver
Status
Billable / Specific
Parent Code
Q44.7Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Accessory liver
- Congenital absence of liver
- Congenital hepatomegaly
Excludes 2
Conditions not included here, but the patient may have both
Code Also
A second code may be required; sequencing depends on circumstances
- , if applicable, associated malformations affecting other systems
Related Codes(2)
Also Known As / Clinical Terms(156)
SNOMED CT
- Congenital syphilitic hepatomegaly192008
- Congenital hepatomegaly407000
- Congenital absence of liver3650004
- Agenesis of lobe of liver13630003
- Congenital absence of liver lobe13630003
- Congenital absence of lobe of liver13630003
- Congenital liver grooves20919000
- Cirrhosis of pancreas25942009
- Fibrosis of pancreas25942009
- Floating liver40210001
- Congenital hyperplasia of muscle66042003
- Congenital muscular hypertrophy66042003
- Doppellendigkeit66042003
- Myofibrillar hyperplasia66042003
- Accessory liver71728002
- Congenital duplication of liver79552009
- Duplication of liver79552009
- Congenital hepatic fibrosis79607001
- Microhepatia85700008
- Atrophy of liver89835009
- Hepatic atrophy89835009
- Congenital abnormal fusion of liver lobes92864004
- Congenital abnormal liver lobation92864004
- Congenital abnormal shape of liver92924002
- Congenital misshapen liver92924002
- Congenital malposition of liver93332007
- Congenital malpositioned liver93332007
- Congenital microhepatia93369005
- Congenital small liver93369005
- Supernumerary liver lobe95297004
- Riedel lobe of liver109559009
- Riedel's lobe of liver109559009
- Congenital absence of liver and/or gallbladder204787003
- Congenital atrophy of left lobe of liver204788008
- Liver and/or biliary duplication204790009
- Congenital floating liver204795004
- Liver hyperplasia204799005
- Familial aplasia of the vermis253175003
- Abnormal liver lobulation253811003
- Trilobular liver253812005
- Ectopic liver253813000
- Focal nodular hypoplasia of liver253814006
- Liver in central position447917005
- Liver in left sided position448683002
- Joubert syndrome716997004
- COACH (cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis) syndrome721847002
- COACH syndrome721847002
- Cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis721847002
- Gentile syndrome721847002
- Joubert syndrome with congenital hepatic fibrosis721847002
- Joubert syndrome with hepatic defect721847002
- Ivemark II syndrome763891005
- Renal hepatic pancreatic dysplasia763891005
- Renohepaticopancreatic dysplasia763891005
- Hepatic fibrosis, renal cyst, intellectual disability syndrome771149000
- Thompson Baraitser syndrome771149000
- Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome773584001
- Goldston syndrome773737004
- Meckel syndrome type 7773737004
- Meckel-like syndrome type 1773737004
- NPHP3 (nephrocystin 3) related Meckel-like syndrome773737004
- NPHP3-related Meckel-like syndrome773737004
- Nephrocystin 3-related Meckel-like syndrome773737004
- Renal, hepatic, pancreatic dysplasia, Dandy-Walker cysts syndrome773737004
- Agenesis of liver1003514000
- Congenital complete absence of liver1003514000
- Absence of liver1156870007
- Liver absent1156870007
UMLS
- Accessory liverC2939133
- Accessory liver (disorder)C2939133
- Agenesis of liverC0266258
- Agenesis of liver (disorder)C0266258
- Congenital absence of liverC0266258
- Congenital absence of liver (disorder)C0266258
- Congenital complete absence of liverC0266258
- Failed liver developmentC0266258
- Hepatic agenesisC0266258
- Liver agenesisC0266258
- Congenital hepatomegalyC0266263
- Congenital hepatomegaly (disorder)C0266263
- Other congenital malformations of liverC0478037
Clinical Terms
- Hepatic fibrosis, renal cyst, intellectual disability syndrome
- Familial aplasia of the vermis
- Meckel syndrome type 7
- Atrophy of liver
- Cirrhosis of pancreas
- Congenital absence of liver (disorder)
- Liver agenesis
- Trilobular liver
- Doppellendigkeit
- Riedel's lobe of liver
- Congenital small liver
- Thompson Baraitser syndrome
- Agenesis of liver
- Congenital floating liver
- Congenital malposition of liver
- NPHP3-related Meckel-like syndrome
- Goldston syndrome
- Joubert syndrome
- Renal hepatic pancreatic dysplasia
- Congenital hepatomegaly
- Joubert syndrome with hepatic defect
- Liver hyperplasia
- Congenital complete absence of liver
- Congenital atrophy of left lobe of liver
- Congenital hyperplasia of muscle
- Microhepatia
- Congenital misshapen liver
- Focal nodular hypoplasia of liver
- Congenital absence of liver lobe
- Riedel lobe of liver
- Liver absent
- Meckel-like syndrome type 1
- Absence of liver
- Nephrocystin 3-related Meckel-like syndrome
- Supernumerary liver lobe
- Congenital abnormal liver lobation
- Hepatic agenesis
- Duplication of liver
- Ectopic liver
- Congenital absence of liver
- Congenital abnormal fusion of liver lobes
- Congenital muscular hypertrophy
- Congenital duplication of liver
- Fibrosis of pancreas
- Congenital absence of lobe of liver
- Failed liver development
- COACH syndrome
- Congenital malpositioned liver
- Renohepaticopancreatic dysplasia
- Liver in left sided position
- COACH (cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis) syndrome
- Congenital absence of liver and/or gallbladder
- Abnormal liver lobulation
- Congenital hepatomegaly (disorder)
- Renal, hepatic, pancreatic dysplasia, Dandy-Walker cysts syndrome
- Congenital abnormal shape of liver
- Agenesis of lobe of liver
- Joubert syndrome with congenital hepatic fibrosis
- Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome
- NPHP3 (nephrocystin 3) related Meckel-like syndrome
- Liver and/or biliary duplication
- Accessory liver (disorder)
- Congenital microhepatia
- Floating liver
- Liver in central position
- Congenital syphilitic hepatomegaly
- Agenesis of liver (disorder)
- Hepatic atrophy
- Gentile syndrome
- Congenital hepatic fibrosis
- Congenital liver grooves
- Myofibrillar hyperplasia
- Accessory liver
- Ivemark II syndrome
- Cerebellar vermis hypoplasia, oligophrenia, congenital ataxia, coloboma, hepatic fibrosis
Frequently Asked Questions
What is the ICD-10 code for other congenital malformations of liver?
The ICD-10-CM code for other congenital malformations of liver is Q44.79. The full clinical description is "Other congenital malformations of liver". Q44.79 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q44.79 mean?
ICD-10-CM code Q44.79 represents “Other congenital malformations 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 Q44.79 a billable code?
Yes, Q44.79 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q44.79 in?
Q44.79 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q44.79 map to?
Q44.79 maps to 39 SNOMED CT concepts: 253811003, 1156870007, 71728002, 1003514000, 13630003, and 34 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q44.79?
Q44.79 is linked to 4 UMLS Concept Unique Identifiers: C2939133, C0266258, C0266263, C0478037. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q44.79 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformations 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 Q44.79?
There is no direct ICD-11 mapping available for Q44.79 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.