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 326 for Abnormality of the liver
  1. NPHP1 gene 
    ... involves neurological problems and can include nephronophthisis, eye abnormalities, liver disease, and other abnormalities. As in nephronophthisis type1 ( ...
    https://medlineplus.gov/genetics/gene/nphp1 - Genetics
  2. SLC30A10 gene 
    ... number of red blood cells (polycythemia); and liver abnormalities, including irreversible liver disease (cirrhosis).Mutations in the SLC30A10 gene impair ...
    https://medlineplus.gov/genetics/gene/slc30a10 - Genetics
  3. CPT1A gene 
    ... levels of ammonia in the blood (hyperammonemia), and abnormalities in liver enzymes. A small percentage of women who have ...
    https://medlineplus.gov/genetics/gene/cpt1a - Genetics
  4. Congenital bile acid synthesis defect type 1 
    ... As the condition progresses, affected individuals can develop liver abnormalities including an enlarged liver (hepatomegaly), inflammation, or chronic ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-1 - Genetics
  5. Blood in Urine: MedlinePlus Medical Test 
    ... culture Minemura M, Tajiri K, Shimizu Y. Systemic abnormalities in liver disease. World J Gastroenterol [Internet]. 2009 June 28 [ ...
    https://medlineplus.gov/lab-tests/blood-in-urine - Medical Tests
  6. Congenital bile acid synthesis defect type 2 
    ... As the condition progresses, affected individuals can develop liver abnormalities including inflammation or chronic liver disease (cirrhosis). Some individuals with congenital bile acid ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-2 - Genetics
  7. Fatty Liver (Merck & Co., Inc.)  
    Merck & Co., Inc. ... Fatty Liver - Learn about the causes, symptoms, diagnosis & treatment from the Merck Manuals - Medical Consumer Version. ... NAFLD,NASH,steatohepatitis
    https://www.merckmanuals.com/.../fatty-liver - External Health Links
  8. NGLY1 gene 
    ... affects many body systems, causing delayed development, movement abnormalities, problems with liver function, eye abnormalities, and a reduction or absence ...
    https://medlineplus.gov/genetics/gene/ngly1 - Genetics
  9. Joubert Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    National Institute of Neurological Disorders and Stroke ... Cerebellar Disorders/Specifics ... Cerebellar Disorders ... Joubert syndrome is a rare genetic condition ...
    https://www.ninds.nih.gov/.../disorders/joubert-syndrome - External Health Links
  10. Hypermanganesemia with dystonia 
    ... from manganese buildup in the liver leads to liver abnormalities in people with HMDPC. Because SLC39A14 gene mutations prevent manganese from entering liver cells, people with hypermanganesemia with dystonia 2 do ...
    https://medlineplus.gov/.../hypermanganesemia-with-dystonia - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next