| C0001418 |
BXGD000050 |
Adenocarcinoma |
Neoplasms |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0006868 |
BXGD000415 |
Cannabis Abuse |
Chemically-Induced Disorders; Mental Disorders |
| C0006870 |
BXGD000416 |
Cannabis Dependence |
Chemically-Induced Disorders; Mental Disorders |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0009171 |
BXGD000587 |
Cocaine Abuse |
Chemically-Induced Disorders; Mental Disorders |
| C0011603 |
BXGD000734 |
Dermatitis |
Skin and Connective Tissue Diseases |
| C0017636 |
BXGD001131 |
Glioblastoma |
Neoplasms |
| C0018614 |
BXGD001209 |
Hashish Abuse |
Chemically-Induced Disorders; Mental Disorders |
| C0020443 |
BXGD001385 |
Hypercholesterolemia |
Nutritional and Metabolic Diseases |
| C0020473 |
BXGD001396 |
Hyperlipidemia |
Nutritional and Metabolic Diseases |
| C0023890 |
BXGD001713 |
Liver Cirrhosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0024809 |
BXGD001808 |
Marijuana Abuse |
Chemically-Induced Disorders; Mental Disorders |
| C0025202 |
BXGD001832 |
melanoma |
Neoplasms |
| C0027627 |
BXGD002006 |
Neoplasm Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0028756 |
BXGD002083 |
Obesity, Morbid |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0029531 |
BXGD002164 |
Other cataract |
Eye Diseases |
| C0031391 |
BXGD002302 |
Phencyclidine Abuse |
Chemically-Induced Disorders; Mental Disorders |
| C0033578 |
BXGD002408 |
Prostatic Neoplasms |
Neoplasms; Male Urogenital Diseases |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0037268 |
BXGD002675 |
Skin Abnormalities |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0086543 |
BXGD003294 |
Cataract |
Eye Diseases |
| C0151718 |
BXGD003464 |
Hypocholesterolemia |
Nutritional and Metabolic Diseases |
| C0153676 |
BXGD003679 |
Secondary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0175694 |
BXGD004002 |
Smith-Lemli-Opitz Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0201657 |
BXGD004051 |
C-reactive protein measurement |
|
| C0234398 |
BXGD004664 |
Visual Cortex Disorder |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0236735 |
BXGD004824 |
Cannabis-Related Disorder |
Chemically-Induced Disorders; Mental Disorders |
| C0236736 |
BXGD004825 |
Cocaine-Related Disorders |
Chemically-Induced Disorders; Mental Disorders |
| C0236742 |
BXGD004826 |
Phencyclidine-Related Disorders |
Chemically-Induced Disorders; Mental Disorders |
| C0242379 |
BXGD005157 |
Malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0265267 |
BXGD005492 |
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| C0282102 |
BXGD006795 |
Chondrodysplasia punctata, X-linked dominant type |
Musculoskeletal Diseases |
| C0342731 |
BXGD007535 |
Deficiency of mevalonate kinase |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases |
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0392885 |
BXGD008071 |
High density lipoprotein measurement |
|
| C0398691 |
BXGD008217 |
Hyperimmunoglobulinemia D |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases |
| C0400966 |
BXGD008266 |
Non-alcoholic Fatty Liver Disease |
Digestive System Diseases |
| C0406756 |
BXGD008369 |
Keratolytic winter erythema |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0428472 |
BXGD008630 |
Serum HDL cholesterol measurement |
|
| C0524910 |
BXGD009248 |
Hepatitis C, Chronic |
Digestive System Diseases; Infections |
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C0600427 |
BXGD009706 |
Cocaine Dependence |
Chemically-Induced Disorders; Mental Disorders |
| C0684249 |
BXGD009790 |
Carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0877008 |
BXGD011325 |
Enzyme inhibition disorder |
|
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1306460 |
BXGD012362 |
Primary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C1621958 |
BXGD013468 |
Glioblastoma Multiforme |
Neoplasms |
| C1959626 |
BXGD016644 |
Mevalonic Aciduria |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases |
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2711227 |
BXGD017478 |
Steatohepatitis |
Digestive System Diseases |
| C2931048 |
BXGD017947 |
HEM dysplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C3553450 |
BXGD019175 |
Profound global developmental delay |
|
| C3714756 |
BXGD019429 |
Intellectual Disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C3875321 |
BXGD019874 |
Inflammatory dermatosis |
Skin and Connective Tissue Diseases |
| C4022810 |
BXGD021005 |
Abnormality of nervous system morphology |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C4025871 |
BXGD021839 |
Abnormality of the face |
|
| C4048268 |
BXGD021896 |
Cortical visual impairment |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C4529962 |
BXGD023178 |
Fatty Liver Disease |
|
| C4748427 |
BXGD024001 |
SQUALENE SYNTHASE DEFICIENCY |
|