| C0002871 |
BXGD000132 |
Anemia |
Hemic and Lymphatic Diseases |
| C0002878 |
BXGD000137 |
Anemia, Hemolytic |
Hemic and Lymphatic Diseases |
| C0002881 |
BXGD000140 |
Anemia, Hemolytic, Congenital |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases |
| C0008372 |
BXGD000535 |
Intrahepatic Cholestasis |
Digestive System Diseases |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0020433 |
BXGD001379 |
Hyperbilirubinemia |
Pathological Conditions, Signs and Symptoms |
| C0022346 |
BXGD001537 |
Icterus |
Pathological Conditions, Signs and Symptoms |
| C0023895 |
BXGD001717 |
Liver diseases |
Digestive System Diseases |
| C0268307 |
BXGD005892 |
Conjugated hyperbilirubinemia |
Pathological Conditions, Signs and Symptoms |
| C0860204 |
BXGD011219 |
Cholestatic liver disease |
Digestive System Diseases |
| C1292769 |
BXGD012230 |
Precursor B-cell lymphoblastic leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1321907 |
BXGD012451 |
Congenital absence of parathyroid gland |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases |
| C1845977 |
BXGD014769 |
X- linked recessive |
|
| C4551898 |
BXGD023434 |
Cholestasis, progressive familial intrahepatic 1 |
Digestive System Diseases |
| C4746970 |
BXGD023964 |
HEMOLYTIC ANEMIA, CONGENITAL, X-LINKED |
|