| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0002886 |
BXGD000144 |
Anemia, Macrocytic |
Hemic and Lymphatic Diseases |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0009241 |
BXGD000595 |
Cognition Disorders |
Mental Disorders |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027794 |
BXGD002036 |
Neural Tube Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0035302 |
BXGD002527 |
Retinal Artery Occlusion |
Eye Diseases; Cardiovascular Diseases |
| C0042847 |
BXGD003006 |
Vitamin B 12 Deficiency |
Nutritional and Metabolic Diseases |
| C0268583 |
BXGD005997 |
Methylmalonic acidemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0348484 |
BXGD007874 |
Other disorders of branched-chain amino-acid metabolism |
Nutritional and Metabolic Diseases |
| C0598608 |
BXGD009668 |
Hyperhomocysteinemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0795690 |
BXGD010728 |
Congenital omphalocele |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C1855119 |
BXGD015463 |
Methylmalonic aciduria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C3150900 |
BXGD018352 |
METHYLMALONIC ACIDURIA, TRANSIENT, DUE TO TRANSCOBALAMIN RECEPTOR DEFECT |
|
| C3472614 |
BXGD018922 |
Plasmablastic lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C4722085 |
BXGD023788 |
Malignant neoplasm of colon and/or rectum |
|
| C4749905 |
BXGD024067 |
Methylmalonic aciduria due to transcobalamin receptor defect |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |