Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 14 for Cholestasis
  1. Benign recurrent intrahepatic cholestasis 
    Benign recurrent intrahepatic cholestasis (BRIC) is characterized by episodes of liver dysfunction called cholestasis. During these episodes, the liver cells ...
    https://medlineplus.gov/...benign-recurrent-intrahepatic-cholestasis - Genetics
  2. Intrahepatic cholestasis of pregnancy 
    Intrahepatic cholestasis of pregnancy (also called ICP) is a liver disorder that typically occurs during the second half of pregnancy. Cholestasis is a condition that ...
    https://medlineplus.gov/.../intrahepatic-cholestasis-of-pregnancy - Genetics
  3. Progressive familial intrahepatic cholestasis 
    Progressive familial intrahepatic cholestasis (PFIC) is a disorder that causes progressive liver disease, which typically leads to liver failure. In people with PFIC, ...
    https://medlineplus.gov/...ressive-familial-intrahepatic-cholestasis - Genetics
  4. Congenital bile acid synthesis defect type 2 
    ... defect type 2 is a disorder characterized by cholestasis, a condition that impairs the production and release ... show signs and symptoms of the condition. CBAS2 Cholestasis with delta(4)-3-oxosteroid 5-beta-reductase ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-2 - Genetics
  5. GRACILE syndrome 
    ... the condition's characteristic features: growth retardation, aminoaciduria, cholestasis, iron overload, lactic acidosis, and early death.In ... the urine (aminoaciduria). Babies with GRACILE syndrome have cholestasis, which is a reduced ability to produce and ...
    https://medlineplus.gov/genetics/condition/gracile-syndrome - Genetics
  6. Congenital bile acid synthesis defect type 1 
    ... defect type 1 is a disorder characterized by cholestasis, a condition that impairs the production and release ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-1 - Genetics
  7. North American Indian childhood cirrhosis 
    ... Gabbiani G, Morin CL, Roy CC. Severe familial cholestasis in North American Indian children: a clinical model ...
    https://medlineplus.gov/...north-american-indian-childhood-cirrhosis - Genetics
  8. Microvillus inclusion disease 
    ... of the bones (osteoporosis). Some affected individuals develop cholestasis, which is a reduced ability to produce and release a digestive fluid called bile. Cholestasis leads to irreversible liver disease (cirrhosis).In individuals ...
    https://medlineplus.gov/.../condition/microvillus-inclusion-disease - Genetics
  9. Alagille syndrome 
    ... Alagille-Watson syndrome Arteriohepatic dysplasia (AHD) Cardiovertebral syndrome Cholestasis with peripheral pulmonary stenosis Hepatic ductular hypoplasia Hepatofacioneurocardiovertebral ...
    https://medlineplus.gov/genetics/condition/alagille-syndrome - Genetics
  10. Citrullinemia 
    ... infants had a liver disorder called neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD). This liver condition ... Citrullinemia type II Genetic Testing Registry: Neonatal intrahepatic cholestasis due to citrin deficiency Citrullinemia type I Citrullinemia ...
    https://medlineplus.gov/genetics/condition/citrullinemia - Genetics
previous · 1 · 2 · next