K83.1 - Obstruction of bile duct

Approximate Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

• Ampulla of Vater obstruction syndrome
• Anastomotic biliary stricture
• Anastomotic stricture of small intestine
• Benign intrahepatic cholestasis type 2
• Benign recurrent intrahepatic cholestasis
• Biliary stricture
• Biliary stricture
• Biliary stricture
• Cholestasis
• Cholestasis
• Cholestasis
• Cholestasis
• Cholestasis in newborn
• Cholestasis in newborn
• Cholestasis of pregnancy
• Cholestasis of pregnancy complicating childbirth
• Cholestasis with pigmentary retinopathy and cleft palate syndrome
• Cholestasis-edema syndrome, Norwegian type
• Courvoisier-Terrier syndrome
• Deficiency of coagulation factor due to vitamin K deficiency
• Deficiency of coagulation factor due to vitamin K malabsorption in obstructive biliary disease
• Disorder of anastomosis of biliary tract
• Disorder of liver due to disorder of amino acid metabolism
• Drug-induced intrahepatic cholestasis
• Extrahepatic cholestasis
• Extrahepatic obstructive biliary disease
• GRACILE syndrome
• Intrahepatic cholestasis
• Liver disorder in pregnancy
• Mirizzi's syndrome
• Neonatal intrahepatic cholestasis due to citrin deficiency
• Obstruction of bile duct
• Obstruction of biliary tree
• Obstruction of common bile duct
• Obstructive hyperbilirubinemia
• Occlusion of bile duct
• Postoperative biliary stricture
• Postoperative stricture
• Progressive familial intrahepatic cholestasis type 1
• Progressive familial intrahepatic cholestasis type 2
• Progressive familial intrahepatic cholestasis type 3
• Progressive intrahepatic cholestasis
• Progressive intrahepatic cholestasis
• Retinal pigment deposits
• Stasis of bile duct
• Stenosis of bile duct
• Stenosis of bile duct
• Stenosis of bile duct
• Stenosis of jejunum
• Stenosis of stoma
• Stricture of anastomosis of gastrointestinal tract
• Stricture of anastomosis of intestine
• Stricture of bile duct
• Stricture of bile duct
• Stricture of bile duct
• Stricture of biliary-enteric anastomosis
• Stricture of hepatic duct
• Stricture of hepatic duct
• Stricture of hepaticojejunal anastomosis
• Stricture of jejunum
• Stricture of small intestine
• Vanishing bile duct syndrome
• Vitamin K deficiency coagulation disorder due to malabsorption

Clinical Information

• Alagille Syndrome-. a multisystem disorder that is characterized by aplasia of intrahepatic bile ducts (bile ducts, intrahepatic), and malformations in the cardiovascular system, the eyes, the vertebral column, and the facies. major clinical features include jaundice, and congenital heart disease with peripheral pulmonary stenosis. alagille syndrome may result from heterogeneous gene mutations, including mutations in jag1 on chromosome 20 (type 1) and notch2 on chromosome 1 (type 2).
• Cholestasis-. impairment of bile flow due to obstruction in small bile ducts (intrahepatic cholestasis) or obstruction in large bile ducts (extrahepatic cholestasis).
• Cholestasis, Extrahepatic-. impairment of bile flow in the large bile ducts by mechanical obstruction or stricture due to benign or malignant processes.
• Cholestasis, Intrahepatic-. impairment of bile flow due to injury to the hepatocytes; bile canaliculi; or the intrahepatic bile ducts (bile ducts, intrahepatic).
• Bile Ducts-. the channels that collect and transport the bile secretion from the bile canaliculi, the smallest branch of the biliary tract in the liver, through the bile ductules, the bile ducts out the liver, and to the gallbladder for storage.
• Benign Recurrent Intrahepatic Cholestasis-. reappearance of cholestasis caused by obstruction within the liver by non-cancerous conditions.
• ABCB11 wt Allele|ABC Member 16, MDR/TAP Subfamily Gene|ABC16|ATP Binding Cassette Subfamily B Member 11 wt Allele|ATP-Binding Cassette, Sub-Family B (MDR/TAP), Member 11 Gene|ATP-Binding Cassette, Subfamily B, Member 11 Gene|BRIC2|BSEP|PFIC-2|PFIC2|PGY4|Progressive Familial Intrahepatic Cholestasis 2 Gene|SPGP|Sister of P-Glycoprotein Gene-. human abcb11 wild-type allele is located in the vicinity of 2q24 and is approximately 108 kb in length. this allele, which encodes bile salt export pump protein, is involved in bile salt transport. mutation of the gene is associated with hereditary intrahepatic cholestasis.
• Intrahepatic Cholestasis-. impairment of the bile flow caused by obstruction within the liver.
• Progressive Familial Intrahepatic Cholestasis-. a genetic syndrome affecting infants and children. it is characterized by chronic intrahepatic cholestasis usually progressing to cirrhosis within the first ten years of life.
• Recurrent Intrahepatic Cholestasis-. reappearance of cholestasis caused by obstruction within the liver.

Diagnostic Related Groups - MS-DRG Mapping

The is diagnosis code is grouped in the following groups for version MS-DRG V40.0 What are Diagnostic Related Groups?
The Diagnostic Related Groups (DRGs) are a patient classification scheme which provides a means of relating the type of patients a hospital treats. The DRGs divides all possible principal diagnoses into mutually exclusive principal diagnosis areas referred to as Major Diagnostic Categories (MDC). applicable from 10/01/2022 through 09/30/2023.

Convert to ICD-9 Code

Patient Education

Bile Duct Diseases

Your liver makes a digestive juice called bile. Your gallbladder stores it between meals. When you eat, your gallbladder pushes the bile into tubes called bile ducts. They carry the bile to your small intestine. The bile helps break down fat. It also helps the liver get rid of toxins and wastes.

Different diseases can block the bile ducts and cause a problem with the flow of bile:

• Gallstones, which can increase pressure in the gallbladder and cause a gallbladder attack. The pain usually lasts from one to several hours.
• Cancer
• Infections
• Birth defects, such as biliary atresia. It is the most common reason for liver transplants in children in the United States.
• Inflammation, which can cause scarring. Over time, this can lead to liver failure.

NIH: National Institute of Diabetes and Digestive and Kidney Diseases

Code History

• FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
• FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
• FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
• FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
• FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
• FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
• FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
• FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016 (First year ICD-10-CM implemented into the HIPAA code set)