| C0000768 |
BXGD000007 |
Congenital Abnormality |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0003873 |
BXGD000236 |
Rheumatoid Arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C0005779 |
BXGD000336 |
Blood Coagulation Disorders |
Hemic and Lymphatic Diseases |
| C0008370 |
BXGD000534 |
Cholestasis |
Digestive System Diseases |
| C0008372 |
BXGD000535 |
Intrahepatic Cholestasis |
Digestive System Diseases |
| C0011847 |
BXGD000749 |
Diabetes |
Endocrine System Diseases |
| C0011849 |
BXGD000751 |
Diabetes Mellitus |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011991 |
BXGD000766 |
Diarrhea |
Pathological Conditions, Signs and Symptoms |
| C0015544 |
BXGD001003 |
Failure to Thrive |
Pathological Conditions, Signs and Symptoms |
| C0018995 |
BXGD001265 |
Hemochromatosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0019158 |
BXGD001293 |
Hepatitis |
Digestive System Diseases |
| C0019159 |
BXGD001294 |
Hepatitis A |
Digestive System Diseases; Infections |
| C0019209 |
BXGD001305 |
Hepatomegaly |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0020433 |
BXGD001379 |
Hyperbilirubinemia |
Pathological Conditions, Signs and Symptoms |
| C0022346 |
BXGD001537 |
Icterus |
Pathological Conditions, Signs and Symptoms |
| C0023895 |
BXGD001717 |
Liver diseases |
Digestive System Diseases |
| C0024523 |
BXGD001781 |
Malabsorption Syndrome |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0025517 |
BXGD001875 |
Metabolic Diseases |
Nutritional and Metabolic Diseases |
| C0027051 |
BXGD001963 |
Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0029456 |
BXGD002157 |
Osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0038002 |
BXGD002723 |
Splenomegaly |
Pathological Conditions, Signs and Symptoms |
| C0038238 |
BXGD002741 |
Steatorrhea |
Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0085605 |
BXGD003200 |
Liver Failure |
Digestive System Diseases |
| C0151849 |
BXGD003486 |
Alkaline phosphatase raised |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0392514 |
BXGD008051 |
Hereditary hemochromatosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0400966 |
BXGD008266 |
Non-alcoholic Fatty Liver Disease |
Digestive System Diseases |
| C0424295 |
BXGD008524 |
Hyperactive behavior |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0549613 |
BXGD009390 |
Biliary tract abnormality |
Digestive System Diseases |
| C1291316 |
BXGD012210 |
Deficiency of reductase |
|
| C1314665 |
BXGD012386 |
Serum alkaline phosphatase raised |
|
| C1458140 |
BXGD013134 |
Bleeding tendency |
Hemic and Lymphatic Diseases |
| C1623038 |
BXGD013475 |
Cirrhosis |
Pathological Conditions, Signs and Symptoms |
| C1848701 |
BXGD014967 |
Elevated hepatic transaminase |
|
| C1855106 |
BXGD015459 |
Neonatal onset |
|
| C1856127 |
BXGD015579 |
Bile acid synthesis defect, congenital, 2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases |
| C1859162 |
BXGD015858 |
Neonatal cholestatic liver disease |
|
| C1963165 |
BXGD016685 |
Malabsorption, CTCAE |
|
| C2711227 |
BXGD017478 |
Steatohepatitis |
Digestive System Diseases |
| C2936476 |
BXGD018123 |
Chronic Liver Failure |
Digestive System Diseases |
| C3714745 |
BXGD019427 |
Malabsorption |
Digestive System Diseases |