| C0003850 |
BXGD000225 |
Arteriosclerosis |
Cardiovascular Diseases |
| C0004153 |
BXGD000260 |
Atherosclerosis |
Cardiovascular Diseases |
| C0005586 |
BXGD000315 |
Bipolar Disorder |
Mental Disorders |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007114 |
BXGD000431 |
Malignant neoplasm of skin |
Neoplasms; Skin and Connective Tissue Diseases |
| C0007137 |
BXGD000445 |
Squamous cell carcinoma |
Neoplasms |
| C0023440 |
BXGD001646 |
Acute Erythroblastic Leukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C0023492 |
BXGD001671 |
Leukemia, T-Cell |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027819 |
BXGD002043 |
Neuroblastoma |
Neoplasms |
| C0028259 |
BXGD002073 |
Nodule |
|
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0033806 |
BXGD002428 |
Pseudohypoparathyroidism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0033835 |
BXGD002432 |
Pseudopseudohypoparathyroidism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0037286 |
BXGD002681 |
Skin Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C0040136 |
BXGD002845 |
Thyroid Neoplasm |
Neoplasms; Endocrine System Diseases |
| C0151241 |
BXGD003408 |
Atrial myxoma |
Neoplasms; Cardiovascular Diseases |
| C0406810 |
BXGD008374 |
Carney Complex |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Cardiovascular Diseases |
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0700095 |
BXGD009875 |
Central neuroblastoma |
Neoplasms; Nervous System Diseases |
| C1275592 |
BXGD012088 |
Funisitis (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications |
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1568249 |
BXGD013420 |
Usher Syndrome, Type II |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C2347748 |
BXGD017041 |
Adult Erythroleukemia |
|
| C2931404 |
BXGD018018 |
Albright's hereditary osteodystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C3494506 |
BXGD018968 |
Pseudohypoparathyroidism, Type Ia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C4086165 |
BXGD022126 |
Childhood Neuroblastoma |
Neoplasms |
| C4520840 |
BXGD023041 |
Erythroleukemia (Erythroid/Myeloid) |
Neoplasms; Hemic and Lymphatic Diseases |