Autoimmune hepatitis

Chronic autoimmune hepatitis (AIH) is a rare progressive inflammatory disorder of unknown cause primarily affecting women and associated with circulating autoantibodies, elevated transaminase levels, and increased levels of immunoglobulin.



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Narrow down the case reports



Total: 849 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(61.0%)
30278550
(6181571)
Pernicious anemia associated with cryptogenic cirrhosis: Two case reports and a literature review.
Yan X, Gao R, Hu Y, Jin J.
Medicine (Baltimore). 2018;97(39):e12547.
Cirrhosis Anemia Vitamin B12 deficiency
Adult Aged, 80 and over Anemia, Pernicious Differential Diagnosis Gait Disorders, Neurologic Homo sapiens Liver Cirrhosis Male Neurologic Examination Schilling Test
2
(56.9%)
26390101
A Report of Three Cases With Acquired Generalized Lipodystrophy With Distinct Autoimmune Conditions Treated With Metreleptin.
Lebastchi J, Ajluni N, Neidert A, Oral EA.
J Clin Endocrinol Metab. 2015;100(11):3967-70.
Insulin resistance Urticaria Hepatosplenomegaly Hemolytic anemia
Autoimmune Chronic Hepatitis Autoimmune Diseases Child Compassionate Use Trials Dermatomyositis Females Graves Disease Homo sapiens Hypoglycemic Agents Hypolipidemic Agents Lipodystrophy Male Severity of Illness Index Urticaria
3
(54.4%)
28858213
(5618200)
Recreational Exposure during Algal Bloom in Carrasco Beach, Uruguay: A Liver Failure Case Report.
Vidal F, Sedan D, D'Agostino D, Cavalieri ML, Mullen E, Parot Varela MM, Flores C, Caixach J, Andrinolo D.
Toxins (Basel). 2017;9(9):.
Jaundice Anemia Hepatomegaly
Alanine Transaminase Aspartate Transaminase Bathing Beaches Bilirubin Environmental Exposure Females Harmful Algal Bloom Homo sapiens Infant Liver Liver Failure Microcystins Uruguay Water Pollutants
3
(54.4%)
17569152
An overlap syndrome involving autoimmune hepatitis and systemic lupus erythematosus in childhood.
Usta Y, Gurakan F, Akcoren Z, Ozen S.
World J Gastroenterol. 2007;13(19):2764-7.
Jaundice Hepatosplenomegaly Coombs-positive hemolytic anemia
Autoimmune Chronic Hepatitis Biopsy Child Females Homo sapiens Kidney Liver Lupus Erythematosus, Systemic Syndrome
5
(53.7%)
3758517
'Acute' autoimmune hepatitis.
Crapper RM, Bhathal PS, Mackay IR, Frazer IH.
Digestion. 1986;34(3):216-25.
Urticaria Fever Lymphadenopathy Coombs-positive hemolytic anemia
Adult Autoimmune Diseases Females Hepatitis, Chronic Homo sapiens Liver Time Factors
6
(53.3%)
10536482
[An infant of autoimmune hepatitis (type I) with cirrhosis].
Nakashima S, Kurozumi H, Imagawa T, Miyamae T, Ito S, Inui A, Fujisawa T, Yokota S.
Ryumachi. 1999;39(4):651-6.
Cirrhosis Cholestasis Anemia Fever
Autoimmune Chronic Hepatitis Child Homo sapiens Immunosuppressive Agents Liver Cirrhosis Male
7
(48.8%)
20731114
[Severe disseminated constrictive polyserositis in a patient with rheumatoid arthritis].
Blagova OV, Tsaregorodtsev DA, Nedostup AV, Maevskaia IV, Petukhova NV, Troitskaia MP, Shadaniia IaR.
Ter Arkh. 2010;82(6):56-61.
Edema Cholestasis Thromboembolism Hepatomegaly
Differential Diagnosis Electrocardiography Henoch-Schoenlein Purpura Homo sapiens Male Middle Aged Pericarditis, Constrictive Pleurisy Pulmonary Embolism Rheumatoid Arthritis Serositis Severity of Illness Index
8
(48.7%)
16263818
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome with renal failure: impact of posttransplant immunosuppression on disease activity.
Ulinski T, Perrin L, Morris M, Houang M, Cabrol S, Grapin C, Chabbert-Buffet N, Bensman A, Deschenes G, Giurgea I.
J Clin Endocrinol Metab. 2006;91(1):192-5.
Diabetes mellitus Vitiligo Exocrine pancreatic insufficiency Anemia
AIRE
g|DEL|424_2157|1734
Anti-Inflammatory Agents Child, Preschool Exons Females Gene Deletion Graft Rejection Homo sapiens Immunosuppressive Agents Kidney Failure, Chronic Kidney Transplantation Polyendocrinopathies, Autoimmune Seizures T-Lymphocyte
9
(48.0%)
26648811
(4665353)
Presence of anti-mitochondrial antibodies and elevated serum immunoglobulin G levels: is this primary biliary cirrhosis-autoimmune hepatitis overlap syndrome?
Muttaqillah NA, Abdul Wahab A, Ding CH, Mohammad M, Biswas S, Rahman MM.
EXCLI J. 2015;14:175-8.
Jaundice Hypochromic microcytic anemia
9
(48.0%)
15492611
Rapid progression of autoimmune hepatitis in the background of primary sclerosing cholangitis.
Hong-Curtis J, Yeh MM, Jain D, Lee JH.
J Clin Gastroenterol. 2004;38(10):906-9.
Jaundice Hemolytic anemia
Adult Autoimmune Chronic Hepatitis Biopsy Blood Chemical Analysis Cholangitis, Sclerosing Disease Progression Endoscopic Retrograde Cholangiopancreatography Females Glucocorticoids Homo sapiens Liver Liver Function Tests Ulcerative Colitis
        

Phenotype(s) retrieved from Orphanet

    Total: 32

HPO ID Term Frequency
HP:0003237 Increased circulating IgG level Obligate (100%)
HP:0010702 Increased antibody level in blood Obligate (100%)
HP:0002910 Elevated hepatic transaminase Very frequent (99-80%)
HP:0003262 Smooth muscle antibody positivity Very frequent (99-80%)
HP:0003453 Antineutrophil antibody positivity Very frequent (99-80%)
HP:0003493 Antinuclear antibody positivity Very frequent (99-80%)
HP:0030908 Liver kidney microsome type 1 antibody positivity Very frequent (99-80%)
HP:0030909 Anti-liver cytosolic antigen type 1 antibody positivity Very frequent (99-80%)
HP:0000716 Depressivity Frequent (79-30%)
HP:0002027 Abdominal pain Frequent (79-30%)
HP:0002829 Arthralgia Frequent (79-30%)
HP:0012432 Chronic fatigue Frequent (79-30%)
HP:0012522 Spider hemangioma Frequent (79-30%)
HP:0000099 Glomerulonephritis Occasional (29-5%)
HP:0000739 Anxiety Occasional (29-5%)
HP:0000952 Jaundice Occasional (29-5%)
HP:0001045 Vitiligo Occasional (29-5%)
HP:0001369 Arthritis Occasional (29-5%)
HP:0001394 Cirrhosis Occasional (29-5%)
HP:0001541 Ascites Occasional (29-5%)
HP:0001744 Splenomegaly Occasional (29-5%)
HP:0002037 Inflammation of the large intestine Occasional (29-5%)
HP:0002239 Gastrointestinal hemorrhage Occasional (29-5%)
HP:0003573 Increased total bilirubin Occasional (29-5%)
HP:0006555 Diffuse hepatic steatosis Occasional (29-5%)
HP:0030991 Sclerosing cholangitis Occasional (29-5%)
HP:0100279 Ulcerative colitis Occasional (29-5%)
HP:0100646 Thyroiditis Occasional (29-5%)
HP:0200119 Acute hepatitis Occasional (29-5%)
HP:0001402 Hepatocellular carcinoma Very rare (4-1%)
HP:0004787 Fulminant hepatitis Very rare (4-1%)
HP:0006562 Viral hepatitis Very rare (4-1%)


Phenotype(s) retrieved from case reports

    Total: 166

HPO ID Term # of case reports
HP:0012115 Hepatitis 115
HP:0001394 Cirrhosis 68
HP:0200123 Chronic hepatitis 43
HP:0006562 Viral hepatitis 37
HP:0200119 Acute hepatitis 22
HP:0100646 Thyroiditis 18
HP:0030151 Cholangitis 15
HP:0100279 Ulcerative colitis 15
HP:0001396 Cholestasis 12
HP:0032220 Interface hepatitis 12
HP:0000819 Diabetes mellitus 10
HP:0000821 Hypothyroidism 10
HP:0000979 Purpura 10
HP:0001369 Arthritis 9
HP:0001370 Rheumatoid arthritis 9
HP:0001945 Fever 9
HP:0000952 Jaundice 8
HP:0200120 Chronic active hepatitis 7
HP:0001045 Vitiligo 6
HP:0001873 Thrombocytopenia 6
HP:0002960 Autoimmunity 6
HP:0200084 Giant cell hepatitis 6
HP:0001399 Hepatic failure 5
HP:0001409 Portal hypertension 5
HP:0002090 Pneumonia 5
HP:0002721 Immunodeficiency 5
HP:0000099 Glomerulonephritis 4
HP:0000100 Nephrotic syndrome 4
HP:0000112 Nephropathy 4
HP:0001876 Pancytopenia 4
HP:0002904 Hyperbilirubinemia 4
HP:0005263 Gastritis 4
HP:0000123 Nephritis 3
HP:0001880 Eosinophilia 3
HP:0002014 Diarrhea 3
HP:0002028 Chronic diarrhea 3
HP:0002583 Colitis 3
HP:0002829 Arthralgia 3
HP:0010783 Erythema 3
HP:0032204 Chronic active Epstein-Barr virus infection 3
HP:0100806 Sepsis 3
HP:0000822 Hypertension 2
HP:0000829 Hypoparathyroidism 2
HP:0000872 Hashimoto thyroiditis 2
HP:0000964 Eczema 2
HP:0000998 Hypertrichosis 2
HP:0001025 Urticaria 2
HP:0001395 Hepatic fibrosis 2
HP:0001433 Hepatosplenomegaly 2
HP:0001508 Failure to thrive 2
HP:0001733 Pancreatitis 2
HP:0001735 Acute pancreatitis 2
HP:0001744 Splenomegaly 2
HP:0001875 Neutropenia 2
HP:0001878 Hemolytic anemia 2
HP:0001903 Anemia 2
HP:0002024 Malabsorption 2
HP:0002027 Abdominal pain 2
HP:0002040 Esophageal varix 2
HP:0002155 Hypertriglyceridemia 2
HP:0002240 Hepatomegaly 2
HP:0002586 Peritonitis 2
HP:0003326 Myalgia 2
HP:0004322 Short stature 2
HP:0004787 Fulminant hepatitis 2
HP:0006515 Interstitial pneumonitis 2
HP:0012156 Hemophagocytosis 2
HP:0012234 Agranulocytosis 2
HP:0012432 Chronic fatigue 2
HP:0012819 Myocarditis 2
HP:0025143 Chills 2
HP:0025300 Malar rash 2
HP:0030731 Carcinoma 2
HP:0100785 Insomnia 2
HP:0000096 Glomerulosclerosis 1
HP:0000131 Uterine leiomyoma 1
HP:0000491 Keratitis 1
HP:0000709 Psychosis 1
HP:0000790 Hematuria 1
HP:0000842 Hyperinsulinemia 1
HP:0000926 Platyspondyly 1
HP:0000956 Acanthosis nigricans 1
HP:0000969 Edema 1
HP:0000988 Skin rash 1
HP:0001007 Hirsutism 1
HP:0001009 Telangiectasia 1
HP:0001047 Atopic dermatitis 1
HP:0001096 Keratoconjunctivitis 1
HP:0001097 Keratoconjunctivitis sicca 1
HP:0001271 Polyneuropathy 1
HP:0001298 Encephalopathy 1
HP:0001404 Hepatocellular necrosis 1
HP:0001406 Intrahepatic cholestasis 1
HP:0001413 Micronodular cirrhosis 1
HP:0001513 Obesity 1
HP:0001541 Ascites 1
HP:0001635 Congestive heart failure 1
HP:0001738 Exocrine pancreatic insufficiency 1
HP:0001909 Leukemia 1
HP:0001952 Glucose intolerance 1
HP:0002013 Vomiting 1
HP:0002018 Nausea 1
HP:0002063 Rigidity 1
HP:0002072 Chorea 1
HP:0002098 Respiratory distress 1
HP:0002206 Pulmonary fibrosis 1
HP:0002315 Headache 1
HP:0002329 Drowsiness 1
HP:0002480 Hepatic encephalopathy 1
HP:0002570 Steatorrhea 1
HP:0002584 Intestinal bleeding 1
HP:0002835 Aspiration 1
HP:0002878 Respiratory failure 1
HP:0002902 Hyponatremia 1
HP:0002923 Rheumatoid factor positive 1
HP:0003040 Arthropathy 1
HP:0003077 Hyperlipidemia 1
HP:0003201 Rhabdomyolysis 1
HP:0003270 Abdominal distention 1
HP:0003761 Calcinosis 1
HP:0004389 Intestinal pseudo-obstruction 1
HP:0004420 Arterial thrombosis 1
HP:0004936 Venous thrombosis 1
HP:0005912 Biliary atresia 1
HP:0008404 Nail dystrophy 1
HP:0009830 Peripheral neuropathy 1
HP:0011134 Low-grade fever 1
HP:0011838 Sclerodactyly 1
HP:0011946 Bronchiolitis obliterans 1
HP:0011950 Bronchiolitis 1
HP:0011974 Myelofibrosis 1
HP:0012089 Arteritis 1
HP:0012219 Erythema nodosum 1
HP:0012223 Splenic rupture 1
HP:0012334 Extrahepatic cholestasis 1
HP:0012378 Fatigue 1
HP:0012490 Panniculitis 1
HP:0012578 Membranous nephropathy 1
HP:0012722 Heart block 1
HP:0012735 Cough 1
HP:0025059 Splenic abscess 1
HP:0025474 Erythematous plaque 1
HP:0030050 Narcolepsy 1
HP:0030242 Portal vein thrombosis 1
HP:0030717 Meconium peritonitis 1
HP:0030955 Alcoholism 1
HP:0031002 Neuritis 1
HP:0031003 Polyneuritis 1
HP:0031273 Shock 1
HP:0031368 Intestinal perforation 1
HP:0031690 Opportunistic infection 1
HP:0031925 Rosette 1
HP:0040270 Impaired glucose tolerance 1
HP:0100543 Cognitive impairment 1
HP:0100548 Exstrophy 1
HP:0100583 Corneal perforation 1
HP:0100584 Endocarditis 1
HP:0100614 Myositis 1
HP:0100651 Type I diabetes mellitus 1
HP:0100749 Chest pain 1
HP:0100778 Cryoglobulinemia 1
HP:0100827 Lymphocytosis 1
HP:0200034 Papule 1
HP:0200036 Skin nodule 1
HP:0200042 Skin ulcer 1
HP:0500167 Hypergastrinemia 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID