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
- inborn errors of metabolism (E70-E88)
Code Also
A second code may be required; sequencing depends on circumstances
- , if applicable, associated malformations affecting other systems
Also Known As / Clinical Terms
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
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.
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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.