| C0005586 |
BXGD000315 |
Bipolar Disorder |
Mental Disorders |
| C0013080 |
BXGD000797 |
Down Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0015745 |
BXGD001019 |
Feeding behaviors |
Behavior and Behavior Mechanisms |
| C0023418 |
BXGD001642 |
leukemia |
Neoplasms |
| C0023449 |
BXGD001650 |
Acute lymphocytic leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023452 |
BXGD001651 |
Childhood Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023467 |
BXGD001658 |
Leukemia, Myelocytic, Acute |
Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0268583 |
BXGD005997 |
Methylmalonic acidemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0751072 |
BXGD010312 |
Frontotemporal Lobar Degeneration |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C0751606 |
BXGD010523 |
Adult Acute Lymphocytic Leukemia |
|
| C1332977 |
BXGD012569 |
Childhood Leukemia |
Neoplasms |
| C1337013 |
BXGD012876 |
Differentiated Thyroid Gland Carcinoma |
|
| C1834304 |
BXGD013965 |
AMYOTROPHY, HEREDITARY NEURALGIC |
Nervous System Diseases |
| C1855119 |
BXGD015463 |
Methylmalonic aciduria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C1961102 |
BXGD016673 |
Precursor Cell Lymphoblastic Leukemia Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C3811918 |
BXGD019664 |
GRN-related frontotemporal dementia |
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders |
| C3888194 |
BXGD019955 |
MIXED LINEAGE LEUKEMIA |
|
| C4521042 |
BXGD023055 |
Complete Trisomy 21 Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C4722172 |
BXGD023791 |
Primary differentiated carcinoma of thyroid gland |
|