| C0003873 |
BXGD000236 |
Rheumatoid Arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C0004134 |
BXGD000256 |
Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0005612 |
BXGD000317 |
Birth Weight |
Pathological Conditions, Signs and Symptoms |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007758 |
BXGD000475 |
Cerebellar Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0011854 |
BXGD000753 |
Diabetes Mellitus, Insulin-Dependent |
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases |
| C0017665 |
BXGD001141 |
Membranous glomerulonephritis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases |
| C0019618 |
BXGD001339 |
Histiocytosis |
Hemic and Lymphatic Diseases |
| C0026764 |
BXGD001928 |
Multiple Myeloma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases |
| C0026769 |
BXGD001930 |
Multiple Sclerosis |
Immune System Diseases; Nervous System Diseases |
| C0026838 |
BXGD001938 |
Muscle Spasticity |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027819 |
BXGD002043 |
Neuroblastoma |
Neoplasms |
| C0027877 |
BXGD002055 |
Neuronal Ceroid-Lipofuscinoses |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0033578 |
BXGD002408 |
Prostatic Neoplasms |
Neoplasms; Male Urogenital Diseases |
| C0034067 |
BXGD002456 |
Pulmonary Emphysema |
Respiratory Tract Diseases |
| C0042900 |
BXGD003012 |
Vitiligo |
Skin and Connective Tissue Diseases |
| C0085078 |
BXGD003118 |
Lysosomal Storage Diseases |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0202177 |
BXGD004079 |
Phospholipid measurement |
|
| C0231921 |
BXGD004530 |
Pulmonary function |
|
| C0268281 |
BXGD005882 |
Infantile neuronal ceroid lipofuscinosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0398597 |
BXGD008198 |
Histiocytic syndrome |
Immune System Diseases; Hemic and Lymphatic Diseases |
| C0524851 |
BXGD009246 |
Neurodegenerative Disorders |
Nervous System Diseases |
| C1281901 |
BXGD012133 |
Fatty acid measurement |
|
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C2985280 |
BXGD018223 |
Blood Protein Measurement |
|
| C3160731 |
BXGD018470 |
Pulmonary function (finding) |
|