| C0005684 |
BXGD000319 |
Malignant neoplasm of urinary bladder |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0005695 |
BXGD000323 |
Bladder Neoplasm |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0007102 |
BXGD000425 |
Malignant tumor of colon |
Digestive System Diseases; Neoplasms |
| C0007131 |
BXGD000441 |
Non-Small Cell Lung Carcinoma |
Neoplasms; Respiratory Tract Diseases |
| C0013336 |
BXGD000815 |
Dwarfism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0017536 |
BXGD001114 |
Giardiasis |
Digestive System Diseases; Infections |
| C0017919 |
BXGD001150 |
Glycogen Storage Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0017921 |
BXGD001152 |
Glycogen storage disease type II |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0017922 |
BXGD001153 |
Glycogen Storage Disease Type III |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0019196 |
BXGD001301 |
Hepatitis C |
Digestive System Diseases; Infections |
| C0019209 |
BXGD001305 |
Hepatomegaly |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0020473 |
BXGD001396 |
Hyperlipidemia |
Nutritional and Metabolic Diseases |
| C0020557 |
BXGD001432 |
Hypertriglyceridemia |
Nutritional and Metabolic Diseases |
| C0020615 |
BXGD001445 |
Hypoglycemia |
Nutritional and Metabolic Diseases |
| C0021051 |
BXGD001475 |
Immunologic Deficiency Syndromes |
Immune System Diseases |
| C0023487 |
BXGD001669 |
Acute Promyelocytic Leukemia |
Neoplasms |
| C0023787 |
BXGD001698 |
Lipodystrophy |
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0023893 |
BXGD001716 |
Liver Cirrhosis, Experimental |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0025517 |
BXGD001875 |
Metabolic Diseases |
Nutritional and Metabolic Diseases |
| C0026106 |
BXGD001889 |
Mild Mental Retardation |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0026848 |
BXGD001941 |
Myopathy |
Musculoskeletal Diseases; Nervous System Diseases |
| C0026850 |
BXGD001942 |
Muscular Dystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C0027055 |
BXGD001964 |
Myocardial Reperfusion Injury |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0030326 |
BXGD002209 |
Panniculitis |
Skin and Connective Tissue Diseases |
| C0030552 |
BXGD002238 |
Paresis |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0041948 |
BXGD002939 |
Uremia |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0151786 |
BXGD003475 |
Muscle Weakness |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0220989 |
BXGD004353 |
Acquired partial lipodystrophy |
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0221032 |
BXGD004374 |
Familial generalized lipodystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0239946 |
BXGD005010 |
Fibrosis, Liver |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0241005 |
BXGD005072 |
Creatine phosphokinase serum increased |
|
| C0271694 |
BXGD006239 |
Familial partial lipodystrophy |
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0340279 |
BXGD007314 |
Ventricular hypertrophy |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0349588 |
BXGD007933 |
Short stature |
|
| C0369183 |
BXGD007960 |
Erythrocyte Mean Corpuscular Hemoglobin Test |
|
| C0423224 |
BXGD008475 |
Sunken eyes |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0426429 |
BXGD008564 |
Broad nasal tip |
|
| C0578038 |
BXGD009542 |
Thin lips |
|
| C0699790 |
BXGD009866 |
Colon Carcinoma |
Digestive System Diseases; Neoplasms |
| C0699885 |
BXGD009869 |
Carcinoma of bladder |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0878544 |
BXGD011368 |
Cardiomyopathies |
Cardiovascular Diseases |
| C1261502 |
BXGD011856 |
Finding of Mean Corpuscular Hemoglobin |
|
| C1836542 |
BXGD014129 |
Depressed nasal bridge |
|
| C1848701 |
BXGD014967 |
Elevated hepatic transaminase |
|
| C1848736 |
BXGD014970 |
Distal amyotrophy |
|
| C1853242 |
BXGD015322 |
Midface retrusion |
|
| C1858085 |
BXGD015770 |
Malar flattening |
|
| C1859592 |
BXGD015912 |
ATRICHIA WITH PAPULAR LESIONS |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C1865017 |
BXGD016283 |
Thin upper lip vermilion |
|
| C1866231 |
BXGD016388 |
Full cheeks |
|
| C1968739 |
BXGD016731 |
Glycogen Storage Disease IIIA |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C1968740 |
BXGD016732 |
Glycogen Storage Disease IIIB |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C1968741 |
BXGD016733 |
Glycogen Storage Disease IIIC |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C2919142 |
BXGD017867 |
Short Stature, CTCAE |
|
| C2936915 |
BXGD018152 |
Amylo-1,6-glucosidase deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C3695006 |
BXGD019341 |
GLYCOGEN STORAGE DISEASE, TYPE IIIb |
|
| C3695007 |
BXGD019342 |
GLYCOGEN STORAGE DISEASE, TYPE IIIa |
|
| C4316789 |
BXGD022698 |
Partial lipodystrophy |
Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |