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Jaundice Familial Obstructive Of Infancy C1839927

Published: July 22, 2026Updated: August 20, 2026

A rare liver condition in newborns where bile ducts are blocked, causing jaundice and liver damage. Surgery or liver transplant may be needed.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
K76.9
ICD-11
DA00.0
Body system
hepatobiliary
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Failure to thrive

Generalized symptoms

(hepatobiliary)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Neonatal jaundice

(hepatobiliary)

Dark urine

(hepatobiliary)

Pale stools

(hepatobiliary)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

Standard diagnostic workup

Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]

Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]

Treatment options

Evidence-based approaches to managing this condition.

First-line treatments

1

Hepatoportoenterostomy (Kasai procedure)

Surgical bypass procedure to restore bile flow from the liver to the intestine by connecting the hepatic porta to a loop of intestine, most effective when performed before 60 days of age.

surgical
2

Medication management with follow-up

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
3

Choleretic and supportive therapy

Medical management including ursodeoxycholic acid to promote bile flow, fat-soluble vitamin supplementation, and management of cholestasis symptoms.

medication

Additional treatment options

Specialized nutritional support

Nutritional management with medium-chain triglyceride-enriched formulas to improve fat absorption, address malabsorption, and support normal growth and development.

dietary

Liver function and growth monitoring

Regular assessment of liver function tests, bilirubin levels, nutritional status, and growth parameters to evaluate disease progression and treatment response.

monitoring

Liver transplant evaluation

Assessment for liver transplantation candidacy in cases of progressive liver failure, failed Kasai procedure, or complications of portal hypertension.

surgical

When to seek medical help

Recognize when you need immediate medical attention.

See a doctor within 24 hours

Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.

Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Jaundice Familial Obstructive Of Infancy C1839927?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Medication Comparisons

Compare medications used to treat Jaundice Familial Obstructive Of Infancy C1839927. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy