| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0033578 |
BXGD002408 |
Prostatic Neoplasms |
Neoplasms; Male Urogenital Diseases |
| C0033860 |
BXGD002438 |
Psoriasis |
Skin and Connective Tissue Diseases |
| C0036346 |
BXGD002602 |
Schizophrenia, Childhood |
Mental Disorders |
| C0162309 |
BXGD003934 |
Adrenoleukodystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases |
| C0263361 |
BXGD005292 |
Psoriasis vulgaris |
Skin and Connective Tissue Diseases |
| C0279565 |
BXGD006638 |
Invasive Lobular Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0282525 |
BXGD006809 |
Adrenoleukodystrophy, Neonatal |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0282526 |
BXGD006810 |
Hyperpipecolic Acidemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0282528 |
BXGD006812 |
Peroxisomal Disorders |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0343055 |
BXGD007593 |
Generalized pustular psoriasis |
Skin and Connective Tissue Diseases |
| C0428886 |
BXGD008640 |
Mean blood pressure |
|
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0751708 |
BXGD010560 |
Peroxisomal Dysfunction, General |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0751709 |
BXGD010561 |
Peroxisomal Dysfunction, Multiple |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0751710 |
BXGD010562 |
Peroxisomal Dysfunction, Single |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C1269683 |
BXGD012001 |
Major Depressive Disorder |
Mental Disorders |
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1449563 |
BXGD013086 |
Cardiomyopathy, Familial Idiopathic |
Cardiovascular Diseases |
| C1832200 |
BXGD013810 |
Peroxisome biogenesis disorders |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C4528257 |
BXGD023159 |
Corpuscular Hemoglobin Concentration Mean |
|