| C0000768 |
BXGD000007 |
Congenital Abnormality |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0000846 |
BXGD000015 |
Agenesis |
|
| C0002152 |
BXGD000104 |
Alloxan Diabetes |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0003635 |
BXGD000214 |
Apraxias |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0003850 |
BXGD000225 |
Arteriosclerosis |
Cardiovascular Diseases |
| C0003873 |
BXGD000236 |
Rheumatoid Arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C0003886 |
BXGD000238 |
Arthrogryposis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0004134 |
BXGD000256 |
Ataxia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0004153 |
BXGD000260 |
Atherosclerosis |
Cardiovascular Diseases |
| C0004364 |
BXGD000270 |
Autoimmune Diseases |
Immune System Diseases |
| C0005612 |
BXGD000317 |
Birth Weight |
Pathological Conditions, Signs and Symptoms |
| C0005745 |
BXGD000331 |
Blepharoptosis |
Eye Diseases |
| C0005890 |
BXGD000345 |
Body Height |
|
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0009421 |
BXGD000608 |
Comatose |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0010054 |
BXGD000647 |
Coronary Arteriosclerosis |
Cardiovascular Diseases |
| C0010068 |
BXGD000648 |
Coronary heart disease |
Cardiovascular Diseases |
| C0011175 |
BXGD000701 |
Dehydration |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| 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 |
| C0011854 |
BXGD000753 |
Diabetes Mellitus, Insulin-Dependent |
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases |
| C0011860 |
BXGD000755 |
Diabetes Mellitus, Non-Insulin-Dependent |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011881 |
BXGD000760 |
Diabetic Nephropathy |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C0011884 |
BXGD000762 |
Diabetic Retinopathy |
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases |
| C0013336 |
BXGD000815 |
Dwarfism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0014070 |
BXGD000887 |
Encephalomyelitis |
Infections; Nervous System Diseases |
| C0015544 |
BXGD001003 |
Failure to Thrive |
Pathological Conditions, Signs and Symptoms |
| C0015672 |
BXGD001011 |
Fatigue |
Pathological Conditions, Signs and Symptoms |
| C0015695 |
BXGD001013 |
Fatty Liver |
Digestive System Diseases |
| C0015696 |
BXGD001014 |
Fatty Liver, Alcoholic |
Digestive System Diseases; Chemically-Induced Disorders |
| C0015934 |
BXGD001026 |
Fetal Growth Retardation |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications |
| C0017097 |
BXGD001092 |
Gardner Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms |
| C0017920 |
BXGD001151 |
Glycogen Storage Disease Type I |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0017926 |
BXGD001157 |
Glycogen Storage Disease Type VII |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases |
| C0017979 |
BXGD001159 |
Glycosuria |
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0018798 |
BXGD001223 |
Congenital Heart Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0020456 |
BXGD001392 |
Hyperglycemia |
Nutritional and Metabolic Diseases |
| C0020459 |
BXGD001394 |
Hyperinsulinism |
Nutritional and Metabolic Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020557 |
BXGD001432 |
Hypertriglyceridemia |
Nutritional and Metabolic Diseases |
| C0020615 |
BXGD001445 |
Hypoglycemia |
Nutritional and Metabolic Diseases |
| C0020617 |
BXGD001446 |
Hypoglycemic coma |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Nervous System Diseases; Endocrine System Diseases |
| C0021655 |
BXGD001508 |
Insulin Resistance |
Nutritional and Metabolic Diseases |
| C0021670 |
BXGD001509 |
insulinoma |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0022638 |
BXGD001567 |
Ketosis |
Nutritional and Metabolic Diseases |
| C0022658 |
BXGD001570 |
Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0022716 |
BXGD001579 |
Menkes Kinky Hair Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases |
| C0023281 |
BXGD001628 |
Leishmaniasis |
Infections; Skin and Connective Tissue Diseases |
| C0023890 |
BXGD001713 |
Liver Cirrhosis |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0023893 |
BXGD001716 |
Liver Cirrhosis, Experimental |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0023895 |
BXGD001717 |
Liver diseases |
Digestive System Diseases |
| C0023903 |
BXGD001720 |
Liver neoplasms |
Digestive System Diseases; Neoplasms |
| C0024141 |
BXGD001740 |
Lupus Erythematosus, Systemic |
Skin and Connective Tissue Diseases; Immune System Diseases |
| C0025517 |
BXGD001875 |
Metabolic Diseases |
Nutritional and Metabolic Diseases |
| C0026827 |
BXGD001936 |
Muscle hypotonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0027627 |
BXGD002006 |
Neoplasm Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027773 |
BXGD002035 |
Nesidioblastosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases |
| C0028754 |
BXGD002082 |
Obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0029408 |
BXGD002137 |
Degenerative polyarthritis |
Musculoskeletal Diseases |
| C0032460 |
BXGD002355 |
Polycystic Ovary Syndrome |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0032969 |
BXGD002385 |
Pregnancy in Diabetics |
Female Urogenital Diseases and Pregnancy Complications |
| C0033377 |
BXGD002406 |
Ptosis |
Pathological Conditions, Signs and Symptoms |
| C0035309 |
BXGD002530 |
Retinal Diseases |
Eye Diseases |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0036857 |
BXGD002638 |
Severe intellectual disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0037221 |
BXGD002673 |
Situs Inversus |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0038433 |
BXGD002754 |
Streptozotocin Diabetes |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0041234 |
BXGD002901 |
Chagas Disease |
Infections |
| C0043119 |
BXGD003029 |
Werner Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0085207 |
BXGD003140 |
Gestational Diabetes |
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0085253 |
BXGD003144 |
Adult-Onset Still Disease |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C0085580 |
BXGD003191 |
Essential Hypertension |
Cardiovascular Diseases |
| C0149670 |
BXGD003345 |
Disorder of carbohydrate metabolism |
Nutritional and Metabolic Diseases |
| C0151747 |
BXGD003471 |
Renal tubular disorder |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0151786 |
BXGD003475 |
Muscle Weakness |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0158981 |
BXGD003914 |
Neonatal diabetes mellitus |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0158986 |
BXGD003916 |
Neonatal hypoglycemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0160390 |
BXGD003921 |
Injury of liver |
Digestive System Diseases; Wounds and Injuries |
| C0162275 |
BXGD003924 |
Ketonuria |
Nutritional and Metabolic Diseases |
| C0202236 |
BXGD004086 |
Triglycerides measurement |
|
| C0205734 |
BXGD004115 |
Diabetes, Autoimmune |
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases |
| C0206669 |
BXGD004229 |
Hepatocellular Adenoma |
Digestive System Diseases; Neoplasms |
| C0220630 |
BXGD004302 |
Adult Liver Carcinoma |
Digestive System Diseases; Neoplasms |
| C0220994 |
BXGD004357 |
Hyperammonemia |
Pathological Conditions, Signs and Symptoms |
| C0235974 |
BXGD004796 |
Pancreatic carcinoma |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0235991 |
BXGD004802 |
Small for gestational age (disorder) |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications |
| C0239842 |
BXGD005001 |
Tremor of hands |
|
| C0242339 |
BXGD005150 |
Dyslipidemias |
Nutritional and Metabolic Diseases |
| C0242379 |
BXGD005157 |
Malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0265306 |
BXGD005509 |
Greig cephalopolysyndactyly syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0265610 |
BXGD005555 |
Clinodactyly of fingers |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0266267 |
BXGD005638 |
Congenital hypoplasia of pancreas |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0266589 |
BXGD005698 |
Congenital ear anomaly NOS (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Otorhinolaryngologic Diseases |
| C0267963 |
BXGD005796 |
Exocrine pancreatic insufficiency |
Digestive System Diseases |
| C0268800 |
BXGD006041 |
Simple renal cyst |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0270549 |
BXGD006079 |
Generalized Anxiety Disorder |
Mental Disorders |
| C0271650 |
BXGD006227 |
Impaired glucose tolerance |
Nutritional and Metabolic Diseases |
| C0271702 |
BXGD006241 |
Iatrogenic hyperinsulinism |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C0279000 |
BXGD006622 |
Liver and Intrahepatic Biliary Tract Carcinoma |
Digestive System Diseases; Neoplasms |
| C0300948 |
BXGD006828 |
Caudal Regression Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C0302511 |
BXGD006849 |
Small for gestational age fetus |
Pathological Conditions, Signs and Symptoms |
| C0337438 |
BXGD007159 |
Glucose measurement |
|
| C0339467 |
BXGD007248 |
Proliferative retinopathy |
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases |
| C0342257 |
BXGD007447 |
Complications of Diabetes Mellitus |
Endocrine System Diseases |
| C0342273 |
BXGD007448 |
Transient neonatal diabetes mellitus |
|
| C0342276 |
BXGD007449 |
Maturity onset diabetes mellitus in young |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0342277 |
BXGD007450 |
Diabetes mellitus autosomal dominant type II (disorder) |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0342317 |
BXGD007460 |
Loss of hypoglycemic warning |
|
| C0345904 |
BXGD007745 |
Malignant neoplasm of liver |
Digestive System Diseases; Neoplasms |
| C0346647 |
BXGD007832 |
Malignant neoplasm of pancreas |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0362046 |
BXGD007959 |
Prediabetes syndrome |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0400966 |
BXGD008266 |
Non-alcoholic Fatty Liver Disease |
Digestive System Diseases |
| C0424295 |
BXGD008524 |
Hyperactive behavior |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0428568 |
BXGD008633 |
Fasting blood glucose measurement |
|
| C0442874 |
BXGD008814 |
Neuropathy |
Nervous System Diseases |
| C0494475 |
BXGD009030 |
Tonic - clonic seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0495706 |
BXGD009038 |
elevated blood glucose level |
|
| C0497406 |
BXGD009064 |
Overweight |
Pathological Conditions, Signs and Symptoms |
| C0520947 |
BXGD009126 |
Clumsiness - motor delay |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0523465 |
BXGD009209 |
Serum albumin measurement |
|
| C0524620 |
BXGD009236 |
Metabolic Syndrome X |
Nutritional and Metabolic Diseases |
| C0546884 |
BXGD009345 |
Hypovolemia |
Pathological Conditions, Signs and Symptoms |
| C0557874 |
BXGD009444 |
Global developmental delay |
|
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C0684249 |
BXGD009790 |
Carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0684276 |
BXGD009793 |
Hypsarrhythmia |
Nervous System Diseases |
| C0730345 |
BXGD009960 |
Microalbuminuria |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0742343 |
BXGD010061 |
Acute Chest Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases |
| C0745153 |
BXGD010122 |
Hypoglycaemic episode |
|
| C0856169 |
BXGD011096 |
Endothelial dysfunction |
|
| C0871470 |
BXGD011316 |
Systolic Pressure |
|
| C0877008 |
BXGD011325 |
Enzyme inhibition disorder |
|
| C0877056 |
BXGD011334 |
Hypoglycemic seizures |
Nutritional and Metabolic Diseases |
| C0948089 |
BXGD011504 |
Acute Coronary Syndrome |
Cardiovascular Diseases |
| C0948379 |
BXGD011533 |
Impaired insulin secretion |
|
| C1257958 |
BXGD011816 |
Glucose Metabolism Disorders |
Nutritional and Metabolic Diseases |
| C1261430 |
BXGD011853 |
Fasting blood sugar result |
|
| C1262477 |
BXGD011882 |
Weight decreased |
Pathological Conditions, Signs and Symptoms |
| C1263857 |
BXGD011900 |
Peripheral axonal neuropathy |
Nervous System Diseases |
| C1305855 |
BXGD012348 |
Body mass index |
|
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1306460 |
BXGD012362 |
Primary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C1384666 |
BXGD012948 |
hearing impairment |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C1561643 |
BXGD013363 |
Chronic Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1611743 |
BXGD013456 |
Familial (FPAH) |
|
| C1623038 |
BXGD013475 |
Cirrhosis |
Pathological Conditions, Signs and Symptoms |
| C1720983 |
BXGD013698 |
Channelopathies |
Pathological Conditions, Signs and Symptoms |
| C1833104 |
BXGD013896 |
DIABETES MELLITUS, PERMANENT NEONATAL |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C1836189 |
BXGD014091 |
Radial deviation of finger |
|
| C1838100 |
BXGD014295 |
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 3 (disorder) |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C1840077 |
BXGD014434 |
Anteverted nostril |
|
| C1846288 |
BXGD014796 |
Recurrent hypoglycemia |
Nutritional and Metabolic Diseases |
| C1847425 |
BXGD014865 |
Abnormal oral glucose tolerance |
|
| C1848395 |
BXGD014921 |
Large for gestational age |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications |
| C1849265 |
BXGD015028 |
Overgrowth |
|
| C1853743 |
BXGD015358 |
Muscular hypotonia of the trunk |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1854114 |
BXGD015383 |
Short nose |
|
| C1854301 |
BXGD015391 |
Motor delay |
Mental Disorders |
| C1855520 |
BXGD015506 |
Hyperglycemia, Postprandial |
Nutritional and Metabolic Diseases |
| C1856438 |
BXGD015606 |
Hypoketotic hypoglycemia |
Nutritional and Metabolic Diseases |
| C1856904 |
BXGD015654 |
Reduced pancreatic beta cells |
|
| C1857949 |
BXGD015758 |
Prominent metopic ridge |
|
| C1859523 |
BXGD015908 |
Contractures of the joints of the lower limbs |
|
| C1864903 |
BXGD016270 |
Hyperinsulinemic hypoglycemia |
Nutritional and Metabolic Diseases |
| C1864954 |
BXGD016278 |
Fasting hyperinsulinemia |
Nutritional and Metabolic Diseases |
| C1865014 |
BXGD016282 |
Long philtrum |
|
| C1865290 |
BXGD016305 |
Hyperinsulinemic hypoglycemia, familial, 3 |
Nutritional and Metabolic Diseases |
| C1865916 |
BXGD016355 |
Bilateral ptosis |
Eye Diseases |
| C1866195 |
BXGD016385 |
Downturned corners of mouth |
|
| C1956346 |
BXGD016627 |
Coronary Artery Disease |
Cardiovascular Diseases |
| C1960636 |
BXGD016668 |
Dysglycemia |
|
| C1962966 |
BXGD016678 |
Retinopathy, CTCAE |
|
| C1969875 |
BXGD016798 |
Beta-cell dysfunction |
|
| C1969879 |
BXGD016799 |
Limb joint contracture |
|
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2609269 |
BXGD017176 |
Fasting hyperglycaemia |
|
| C2711227 |
BXGD017478 |
Steatohepatitis |
Digestive System Diseases |
| C2748055 |
BXGD017583 |
Hypoinsulinaemia (disorder) |
|
| C2931689 |
BXGD018049 |
Dystrophia myotonica 2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C2931832 |
BXGD018070 |
Hyperinsulinemic hypoglycemia, familial, 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases |
| C2931833 |
BXGD018071 |
Hyperinsulinemic hypoglycemia, familial, 2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases |
| C2939419 |
BXGD018178 |
Secondary Neoplasm |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C3278636 |
BXGD018744 |
Neonatal insulin-dependent diabetes mellitus |
|
| C3468041 |
BXGD018905 |
FANCONI ANEMIA, COMPLEMENTATION GROUP C |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases |
| C3714756 |
BXGD019429 |
Intellectual Disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C3825462 |
BXGD019697 |
Diabetes in youth |
|
| C3826457 |
BXGD019724 |
Diabetes in children |
|
| C3827793 |
BXGD019739 |
Transient hypothyroxinaemia of prematurity |
|
| C3887499 |
BXGD019884 |
Renal cyst |
Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C3888018 |
BXGD019942 |
Congenital Hyperinsulinism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases |
| C3888631 |
BXGD019983 |
Monogenic diabetes |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C4016117 |
BXGD020277 |
DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET |
|
| C4020778 |
BXGD020480 |
maternal hyperglycemia |
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C4021753 |
BXGD020758 |
Abnormality of the immune system |
|
| C4021759 |
BXGD020762 |
Generalized myoclonic seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C4025714 |
BXGD021750 |
Abnormality of the autonomic nervous system |
|
| C4073162 |
BXGD022053 |
Elevated hemoglobin A1c |
|
| C4280765 |
BXGD022402 |
Abnormal C-peptide level |
|
| C4321446 |
BXGD022751 |
K ATP Permanent Neonatal Diabetes |
|
| C4330695 |
BXGD022806 |
Mitochondrial Diabetes |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C4529962 |
BXGD023178 |
Fatty Liver Disease |
|
| C4551485 |
BXGD023312 |
Clinodactyly |
|
| C4703555 |
BXGD023658 |
Decreased waist to hip ratio |
|
| C4721453 |
BXGD023744 |
Peripheral Nervous System Diseases |
Nervous System Diseases |
| C4728082 |
BXGD023886 |
Severe hypoglycaemia |
|