| C0001430 |
BXGD000054 |
Adenoma |
Neoplasms |
| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0002896 |
BXGD000153 |
Sideroblastic anemia |
Hemic and Lymphatic Diseases |
| C0005586 |
BXGD000315 |
Bipolar Disorder |
Mental Disorders |
| C0011847 |
BXGD000749 |
Diabetes |
Endocrine System Diseases |
| C0011849 |
BXGD000751 |
Diabetes Mellitus |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011853 |
BXGD000752 |
Diabetes Mellitus, Experimental |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011860 |
BXGD000755 |
Diabetes Mellitus, Non-Insulin-Dependent |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0019196 |
BXGD001301 |
Hepatitis C |
Digestive System Diseases; Infections |
| C0020542 |
BXGD001425 |
Pulmonary Hypertension |
Respiratory Tract Diseases |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0032708 |
BXGD002368 |
Disorders of Porphyrin Metabolism |
Nutritional and Metabolic Diseases |
| C0035410 |
BXGD002546 |
Rhabdomyolysis |
Musculoskeletal Diseases |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0162530 |
BXGD003949 |
Porphyria, Erythropoietic |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0162531 |
BXGD003950 |
Hereditary Coproporphyria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0162532 |
BXGD003951 |
Variegate Porphyria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0162557 |
BXGD003956 |
Liver Failure, Acute |
Digestive System Diseases |
| C0162565 |
BXGD003957 |
Acute intermittent porphyria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0162568 |
BXGD003959 |
Erythropoietic Protoporphyria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0235031 |
BXGD004714 |
Neurologic Symptoms |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0243026 |
BXGD005210 |
Sepsis |
Pathological Conditions, Signs and Symptoms; Infections |
| C0271650 |
BXGD006227 |
Impaired glucose tolerance |
Nutritional and Metabolic Diseases |
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C3149631 |
BXGD018283 |
MELORHEOSTOSIS, ISOLATED |
|
| C3203509 |
BXGD018562 |
Neuropsychiatric syndrome |
|