- Q44.7 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM Q44.7 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q44.7 – other international versions of ICD-10 Q44.7 may differ.
ICD-10-CM Q44.7 is grouped within Diagnostic Related Group(s):
- 441 Disorders of liver except malignancy, cirrhosis or alcoholic hepatitis with mcc
- 442 Disorders of liver except malignancy, cirrhosis or alcoholic hepatitis with cc
- 443 Disorders of liver except malignancy, cirrhosis or alcoholic hepatitis without cc/mcc
Applicable To
- Accessory liver
- Alagille’s syndrome
- Congenital absence of liver
- Congenital hepatomegaly
- Congenital malformation of liver NOS
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to Q44.7:
- liver (congenital) > Absence (of) (organ or part) (complete or partial)
- liver > Accessory (congenital)
- hepatic > Agenesis
- liver > Agenesis
- liver > Anomaly, anomalous (congenital) (unspecified type) Q89.9
- liver (congenital) > Deformity Q89.9
- liver > Distortion (s) (congenital)
- liver > Duplication, duplex
- congenital > Hepatomegaly
- liver (congenital) > Hyperplasia, hyperplastic
- congenital > liver R16.0
- liver > Hypoplasia, hypoplastic
- liver, abnormal > Lobulation (congenital)
- liver > Malformation (congenital)
- liver > congenital Q89.1
- lobe, liver > Riedel\’s
- Alagille\’s > Syndrome