| C0002879 |
BXGD000138 |
Anemia, Hemolytic, Acquired |
Hemic and Lymphatic Diseases |
| C0004096 |
BXGD000252 |
Asthma |
Respiratory Tract Diseases; Immune System Diseases |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007102 |
BXGD000425 |
Malignant tumor of colon |
Digestive System Diseases; Neoplasms |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0014544 |
BXGD000926 |
Epilepsy |
Nervous System Diseases |
| C0017658 |
BXGD001138 |
Glomerulonephritis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0018799 |
BXGD001224 |
Heart Diseases |
Cardiovascular Diseases |
| C0019061 |
BXGD001273 |
Hemolytic-Uremic Syndrome |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Hemic and Lymphatic Diseases |
| C0020179 |
BXGD001363 |
Huntington Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders |
| C0022658 |
BXGD001570 |
Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0023890 |
BXGD001713 |
Liver Cirrhosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0027726 |
BXGD002030 |
Nephrotic Syndrome |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0033687 |
BXGD002415 |
Proteinuria |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0034155 |
BXGD002468 |
Purpura, Thrombotic Thrombocytopenic |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0035078 |
BXGD002505 |
Kidney Failure |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0035334 |
BXGD002539 |
Retinitis Pigmentosa |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0040034 |
BXGD002836 |
Thrombocytopenia |
Hemic and Lymphatic Diseases |
| C0155765 |
BXGD003819 |
Disease of capillaries |
Cardiovascular Diseases |
| C0268742 |
BXGD006032 |
Membranoproliferative Glomerulonephritis, Type I |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases |
| C0342782 |
BXGD007549 |
Depletion of mitochondrial DNA |
|
| C0398621 |
BXGD008201 |
Hypoplasminogenemia |
Hemic and Lymphatic Diseases |
| C0424295 |
BXGD008524 |
Hyperactive behavior |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0445347 |
BXGD008819 |
Thickening of glomerular basement membrane |
|
| C0686377 |
BXGD009834 |
CNS metastases |
Neoplasms; Nervous System Diseases |
| C0699790 |
BXGD009866 |
Colon Carcinoma |
Digestive System Diseases; Neoplasms |
| C0814161 |
BXGD010860 |
impaired motor coordination |
|
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1623038 |
BXGD013475 |
Cirrhosis |
Pathological Conditions, Signs and Symptoms |
| C1720821 |
BXGD013685 |
Membranoproliferative Glomerulonephritis, Type III |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases |
| C2316810 |
BXGD017030 |
Chronic kidney disease stage 5 |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C2609414 |
BXGD017182 |
Acute kidney injury |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C2717961 |
BXGD017519 |
Thrombotic Microangiopathies |
Hemic and Lymphatic Diseases |
| C2931788 |
BXGD018064 |
Atypical Hemolytic Uremic Syndrome |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Hemic and Lymphatic Diseases |
| C3554330 |
BXGD019209 |
NEPHROTIC SYNDROME, TYPE 7 |
|
| C3808620 |
BXGD019551 |
HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 7 |
|
| C4055018 |
BXGD021996 |
Familial Atypical Hemolytic Uremic Syndrome |
Pathological Conditions, Signs and Symptoms |
| C4087273 |
BXGD022140 |
C3 glomerulopathy |
|