| C0000772 |
BXGD000009 |
Multiple congenital anomalies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0001206 |
BXGD000033 |
Acromegaly |
Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases |
| C0001403 |
BXGD000048 |
Addison Disease |
Immune System Diseases; Endocrine System Diseases |
| C0001418 |
BXGD000050 |
Adenocarcinoma |
Neoplasms |
| C0001430 |
BXGD000054 |
Adenoma |
Neoplasms |
| C0001618 |
BXGD000063 |
Tumors of Adrenal Cortex |
Neoplasms; Endocrine System Diseases |
| C0001622 |
BXGD000065 |
Adrenal Gland Hyperfunction |
Endocrine System Diseases |
| C0001624 |
BXGD000067 |
Adrenal Gland Neoplasms |
Neoplasms; Endocrine System Diseases |
| C0002382 |
BXGD000109 |
Alveolar Bone Loss |
Musculoskeletal Diseases; Stomatognathic Diseases |
| C0002418 |
BXGD000112 |
Amblyopia |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0002448 |
BXGD000115 |
Ameloblastoma |
Neoplasms |
| C0002871 |
BXGD000132 |
Anemia |
Hemic and Lymphatic Diseases |
| C0003090 |
BXGD000175 |
Ankylosis |
Musculoskeletal Diseases |
| C0003129 |
BXGD000182 |
Anoxemia |
Pathological Conditions, Signs and Symptoms |
| C0003130 |
BXGD000183 |
Anoxia |
Pathological Conditions, Signs and Symptoms |
| C0003467 |
BXGD000194 |
Anxiety |
Behavior and Behavior Mechanisms |
| C0003469 |
BXGD000195 |
Anxiety Disorders |
Mental Disorders |
| C0004096 |
BXGD000252 |
Asthma |
Respiratory Tract Diseases; Immune System Diseases |
| C0004763 |
BXGD000289 |
Barrett Esophagus |
Digestive System Diseases; Neoplasms |
| C0004903 |
BXGD000293 |
Beckwith-Wiedemann Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0005684 |
BXGD000319 |
Malignant neoplasm of urinary bladder |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0005695 |
BXGD000323 |
Bladder Neoplasm |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0005845 |
BXGD000341 |
Blood urea nitrogen measurement |
|
| C0005890 |
BXGD000345 |
Body Height |
|
| C0005940 |
BXGD000352 |
Bone Diseases |
Musculoskeletal Diseases |
| C0005967 |
BXGD000357 |
Bone neoplasms |
Neoplasms; Musculoskeletal Diseases |
| C0006009 |
BXGD000359 |
Borderline intellectual disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0006012 |
BXGD000360 |
Borderline Personality Disorder |
Mental Disorders |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006157 |
BXGD000377 |
Breech Presentation |
Female Urogenital Diseases and Pregnancy Complications |
| C0006287 |
BXGD000390 |
Bronchopulmonary Dysplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases |
| C0006663 |
BXGD000403 |
Calcinosis |
Nutritional and Metabolic Diseases |
| C0006664 |
BXGD000404 |
Calcinosis cutis |
Nutritional and Metabolic Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007095 |
BXGD000423 |
Carcinoid Tumor |
Neoplasms |
| C0007097 |
BXGD000424 |
Carcinoma |
Neoplasms |
| C0007102 |
BXGD000425 |
Malignant tumor of colon |
Digestive System Diseases; Neoplasms |
| C0007115 |
BXGD000432 |
Malignant neoplasm of thyroid |
Neoplasms; Endocrine System Diseases |
| C0007130 |
BXGD000440 |
Mucinous Adenocarcinoma |
Neoplasms |
| C0007131 |
BXGD000441 |
Non-Small Cell Lung Carcinoma |
Neoplasms; Respiratory Tract Diseases |
| C0007133 |
BXGD000442 |
Carcinoma, Papillary |
Neoplasms |
| C0007134 |
BXGD000443 |
Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0007137 |
BXGD000445 |
Squamous cell carcinoma |
Neoplasms |
| C0007138 |
BXGD000446 |
Carcinoma, Transitional Cell |
Neoplasms |
| C0007194 |
BXGD000452 |
Hypertrophic Cardiomyopathy |
Cardiovascular Diseases |
| C0007873 |
BXGD000500 |
Uterine Cervical Neoplasm |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0008031 |
BXGD000511 |
Chest Pain |
Pathological Conditions, Signs and Symptoms |
| C0008073 |
BXGD000518 |
Developmental Disabilities |
Mental Disorders |
| C0008370 |
BXGD000534 |
Cholestasis |
Digestive System Diseases |
| C0009375 |
BXGD000602 |
Colonic Neoplasms |
Digestive System Diseases; Neoplasms |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0009404 |
BXGD000606 |
Colorectal Neoplasms |
Digestive System Diseases; Neoplasms |
| C0009438 |
BXGD000610 |
Common Bile Duct Calculi |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0009676 |
BXGD000619 |
Confusion |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0009763 |
BXGD000628 |
Conjunctivitis |
Eye Diseases |
| C0010278 |
BXGD000660 |
Craniosynostosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0010308 |
BXGD000661 |
Congenital Hypothyroidism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0010481 |
BXGD000673 |
Cushing Syndrome |
Endocrine System Diseases |
| C0010635 |
BXGD000680 |
Cystadenoma, Mucinous |
Neoplasms |
| C0010674 |
BXGD000683 |
Cystic Fibrosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases |
| C0010709 |
BXGD000689 |
Cyst |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0011334 |
BXGD000716 |
Dental caries |
Stomatognathic Diseases |
| C0011351 |
BXGD000717 |
Dental Enamel Hypoplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases |
| C0011573 |
BXGD000730 |
Endogenous depression |
Mental Disorders |
| C0011581 |
BXGD000733 |
Depressive disorder |
Mental Disorders |
| C0011849 |
BXGD000751 |
Diabetes Mellitus |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0011989 |
BXGD000765 |
Camurati-Engelmann Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0011991 |
BXGD000766 |
Diarrhea |
Pathological Conditions, Signs and Symptoms |
| C0013336 |
BXGD000815 |
Dwarfism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0013384 |
BXGD000826 |
Dyskinetic syndrome |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0013404 |
BXGD000833 |
Dyspnea |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
| C0014084 |
BXGD000891 |
Enchondromatosis |
Musculoskeletal Diseases |
| C0014130 |
BXGD000899 |
Endocrine System Diseases |
Endocrine System Diseases |
| C0014859 |
BXGD000961 |
Esophageal Neoplasms |
Digestive System Diseases; Neoplasms |
| C0015544 |
BXGD001003 |
Failure to Thrive |
Pathological Conditions, Signs and Symptoms |
| C0015672 |
BXGD001011 |
Fatigue |
Pathological Conditions, Signs and Symptoms |
| C0015934 |
BXGD001026 |
Fetal Growth Retardation |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications |
| C0015967 |
BXGD001030 |
Fever |
Pathological Conditions, Signs and Symptoms |
| C0016063 |
BXGD001044 |
Osteitis Fibrosa Disseminata |
Musculoskeletal Diseases |
| C0016064 |
BXGD001045 |
Fibrous Dysplasia, Monostotic |
Musculoskeletal Diseases |
| C0016065 |
BXGD001046 |
Polyostotic fibrous dysplasia |
Musculoskeletal Diseases |
| C0016412 |
BXGD001058 |
Folic Acid Deficiency |
Nutritional and Metabolic Diseases |
| C0016663 |
BXGD001071 |
Pathological fracture |
Wounds and Injuries |
| C0017185 |
BXGD001104 |
Gastrointestinal Neoplasms |
Digestive System Diseases; Neoplasms |
| C0017495 |
BXGD001111 |
Gerstmann-Straussler-Scheinker Disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections; Nervous System Diseases |
| C0017601 |
BXGD001125 |
Glaucoma |
Eye Diseases |
| C0017636 |
BXGD001131 |
Glioblastoma |
Neoplasms |
| C0017654 |
BXGD001136 |
Glomerular Filtration Rate |
|
| C0018021 |
BXGD001162 |
Goiter |
Endocrine System Diseases |
| C0018213 |
BXGD001187 |
Graves Disease |
Eye Diseases; Immune System Diseases; Endocrine System Diseases |
| C0018552 |
BXGD001202 |
Hamartoma |
Neoplasms |
| C0018671 |
BXGD001211 |
Head and Neck Neoplasms |
Neoplasms |
| C0018784 |
BXGD001220 |
Sensorineural Hearing Loss (disorder) |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C0019087 |
BXGD001280 |
Hemorrhagic Disorders |
Hemic and Lymphatic Diseases |
| C0020175 |
BXGD001362 |
Hunger |
Behavior and Behavior Mechanisms |
| C0020494 |
BXGD001405 |
Hyperostosis Frontalis Interna |
Musculoskeletal Diseases |
| C0020502 |
BXGD001410 |
Hyperparathyroidism |
Endocrine System Diseases |
| C0020505 |
BXGD001412 |
Hyperphagia |
Pathological Conditions, Signs and Symptoms |
| C0020507 |
BXGD001413 |
Hyperplasia |
Pathological Conditions, Signs and Symptoms |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020550 |
BXGD001429 |
Hyperthyroidism |
Endocrine System Diseases |
| C0020598 |
BXGD001440 |
Hypocalcemia |
Nutritional and Metabolic Diseases |
| C0020619 |
BXGD001447 |
Hypogonadism |
Endocrine System Diseases |
| C0020627 |
BXGD001453 |
Hypopharyngeal Neoplasms |
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| C0020651 |
BXGD001460 |
Hypotension, Orthostatic |
Nervous System Diseases; Cardiovascular Diseases |
| C0020676 |
BXGD001462 |
Hypothyroidism |
Endocrine System Diseases |
| C0020725 |
BXGD001465 |
Type II Mucolipidosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases |
| C0020796 |
BXGD001468 |
Profound Mental Retardation |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0021122 |
BXGD001481 |
Disruptive, Impulse Control, and Conduct Disorders |
Mental Disorders |
| C0021655 |
BXGD001508 |
Insulin Resistance |
Nutritional and Metabolic Diseases |
| C0022107 |
BXGD001530 |
Irritable Mood |
Behavior and Behavior Mechanisms |
| C0022408 |
BXGD001544 |
Arthropathy |
Musculoskeletal Diseases |
| C0022680 |
BXGD001576 |
Polycystic Kidney Diseases |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0022821 |
BXGD001590 |
Kyphosis deformity of spine |
Musculoskeletal Diseases |
| C0023434 |
BXGD001643 |
Chronic Lymphocytic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023827 |
BXGD001707 |
liposarcoma |
Neoplasms |
| C0023895 |
BXGD001717 |
Liver diseases |
Digestive System Diseases |
| C0023897 |
BXGD001719 |
Liver Diseases, Parasitic |
Digestive System Diseases; Infections |
| C0024115 |
BXGD001732 |
Lung diseases |
Respiratory Tract Diseases |
| C0024530 |
BXGD001783 |
Malaria |
Infections |
| C0024623 |
BXGD001791 |
Malignant neoplasm of stomach |
Digestive System Diseases; Neoplasms |
| C0025048 |
BXGD001823 |
Meconium Aspiration Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Respiratory Tract Diseases |
| C0025149 |
BXGD001826 |
Medulloblastoma |
Neoplasms |
| C0025202 |
BXGD001832 |
melanoma |
Neoplasms |
| C0025267 |
BXGD001845 |
Multiple Endocrine Neoplasia Type 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases |
| C0025286 |
BXGD001850 |
Meningioma |
Neoplasms; Nervous System Diseases |
| C0025362 |
BXGD001866 |
Mental Retardation |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0025363 |
BXGD001867 |
Mental Retardation, Psychosocial |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0025517 |
BXGD001875 |
Metabolic Diseases |
Nutritional and Metabolic Diseases |
| C0026948 |
BXGD001952 |
Mycosis Fungoides |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0027086 |
BXGD001970 |
Myoma |
Neoplasms |
| C0027149 |
BXGD001979 |
Myxoma |
Neoplasms |
| C0027627 |
BXGD002006 |
Neoplasm Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027662 |
BXGD002015 |
Multiple Endocrine Neoplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases |
| C0027794 |
BXGD002036 |
Neural Tube Defects |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0027819 |
BXGD002043 |
Neuroblastoma |
Neoplasms |
| C0028738 |
BXGD002081 |
Nystagmus |
Eye Diseases; Nervous System Diseases |
| 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 |
| C0028949 |
BXGD002100 |
Oligomenorrhea |
Pathological Conditions, Signs and Symptoms |
| C0028960 |
BXGD002101 |
Oligospermia |
Male Urogenital Diseases |
| C0029124 |
BXGD002113 |
Optic Atrophy |
Eye Diseases; Nervous System Diseases |
| C0029396 |
BXGD002133 |
Heterotopic Ossification |
Pathological Conditions, Signs and Symptoms |
| C0029408 |
BXGD002137 |
Degenerative polyarthritis |
Musculoskeletal Diseases |
| C0029422 |
BXGD002142 |
Osteochondrodysplasias |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0029438 |
BXGD002148 |
Massive Osteolyses |
Musculoskeletal Diseases |
| C0029440 |
BXGD002149 |
Osteoma |
Neoplasms |
| C0029442 |
BXGD002151 |
Osteomalacia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases; Endocrine System Diseases |
| C0029453 |
BXGD002154 |
Osteopenia |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0029456 |
BXGD002157 |
Osteoporosis |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0029463 |
BXGD002160 |
Osteosarcoma |
Neoplasms |
| C0029464 |
BXGD002161 |
Osteosclerosis |
Musculoskeletal Diseases |
| C0029927 |
BXGD002182 |
Ovarian Cysts |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0030283 |
BXGD002200 |
Pancreatic Cyst |
Digestive System Diseases; Neoplasms |
| C0030297 |
BXGD002204 |
Pancreatic Neoplasm |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0030491 |
BXGD002231 |
Parapsoriasis |
Skin and Connective Tissue Diseases |
| C0030554 |
BXGD002239 |
Paresthesia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0031106 |
BXGD002283 |
Aggressive Periodontitis |
Stomatognathic Diseases |
| C0031269 |
BXGD002297 |
Peutz-Jeghers Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Skin and Connective Tissue Diseases |
| C0031511 |
BXGD002304 |
Pheochromocytoma |
Neoplasms |
| C0031575 |
BXGD002308 |
Phocomelia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0032000 |
BXGD002318 |
Pituitary Adenoma |
Neoplasms; Nervous System Diseases; Endocrine System Diseases |
| C0032460 |
BXGD002355 |
Polycystic Ovary Syndrome |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0032584 |
BXGD002363 |
polyps |
Pathological Conditions, Signs and Symptoms |
| C0032914 |
BXGD002379 |
Pre-Eclampsia |
Female Urogenital Diseases and Pregnancy Complications |
| C0033375 |
BXGD002405 |
Prolactinoma |
Neoplasms; Nervous System Diseases; Endocrine System Diseases |
| C0033578 |
BXGD002408 |
Prostatic Neoplasms |
Neoplasms; Male Urogenital Diseases |
| C0033626 |
BXGD002412 |
Protein Deficiency |
Nutritional and Metabolic Diseases |
| C0033805 |
BXGD002427 |
Pseudohypoaldosteronism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0033806 |
BXGD002428 |
Pseudohypoparathyroidism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0033822 |
BXGD002430 |
Pseudomyxoma Peritonei |
Neoplasms |
| C0033835 |
BXGD002432 |
Pseudopseudohypoparathyroidism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0033975 |
BXGD002447 |
Psychotic Disorders |
Mental Disorders |
| C0034013 |
BXGD002450 |
Precocious Puberty |
Endocrine System Diseases |
| C0035204 |
BXGD002511 |
Respiration Disorders |
Respiratory Tract Diseases |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0037274 |
BXGD002676 |
Dermatologic disorders |
Skin and Connective Tissue Diseases |
| C0037284 |
BXGD002679 |
Skin lesion |
Skin and Connective Tissue Diseases |
| C0037579 |
BXGD002694 |
Soft Tissue Neoplasms |
Neoplasms |
| C0037763 |
BXGD002699 |
Spasm |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0037926 |
BXGD002712 |
Compression of spinal cord |
Nervous System Diseases; Wounds and Injuries |
| C0038379 |
BXGD002752 |
Strabismus |
Eye Diseases; Nervous System Diseases |
| C0038587 |
BXGD002773 |
Substance Withdrawal Syndrome |
Chemically-Induced Disorders; Mental Disorders |
| C0039231 |
BXGD002799 |
Tachycardia |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0039590 |
BXGD002822 |
Testicular Neoplasms |
Neoplasms; Male Urogenital Diseases; Endocrine System Diseases |
| C0039621 |
BXGD002824 |
Tetany |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Nervous System Diseases |
| C0040136 |
BXGD002845 |
Thyroid Neoplasm |
Neoplasms; Endocrine System Diseases |
| C0041408 |
BXGD002923 |
Turner Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases; Cardiovascular Diseases |
| C0042420 |
BXGD002982 |
Vasovagal syncope |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0042514 |
BXGD002989 |
Tachycardia, Ventricular |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0080178 |
BXGD003107 |
Spina Bifida |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0080203 |
BXGD003108 |
Tachyarrhythmia |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0085207 |
BXGD003140 |
Gestational Diabetes |
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0085409 |
BXGD003168 |
Polyendocrinopathies, Autoimmune |
Immune System Diseases; Endocrine System Diseases |
| C0085580 |
BXGD003191 |
Essential Hypertension |
Cardiovascular Diseases |
| C0085583 |
BXGD003194 |
Choreoathetosis |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0085631 |
BXGD003214 |
Agitation |
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0085633 |
BXGD003216 |
Mood swings |
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0085681 |
BXGD003237 |
Hyperphosphatemia (disorder) |
Nutritional and Metabolic Diseases |
| C0085682 |
BXGD003238 |
Hypophosphatemia |
Nutritional and Metabolic Diseases |
| C0086189 |
BXGD003268 |
Drug Withdrawal Symptoms |
Chemically-Induced Disorders; Mental Disorders |
| C0086543 |
BXGD003294 |
Cataract |
Eye Diseases |
| C0087169 |
BXGD003321 |
Withdrawal Symptoms |
Chemically-Induced Disorders; Mental Disorders |
| C0149826 |
BXGD003370 |
Gastric adenoma |
Digestive System Diseases; Neoplasms |
| C0149931 |
BXGD003388 |
Migraine Disorders |
Nervous System Diseases |
| C0151241 |
BXGD003408 |
Atrial myxoma |
Neoplasms; Cardiovascular Diseases |
| C0151468 |
BXGD003424 |
Thyroid Gland Follicular Adenoma |
Neoplasms; Endocrine System Diseases |
| C0151526 |
BXGD003432 |
Premature Birth |
Female Urogenital Diseases and Pregnancy Complications |
| C0151529 |
BXGD003433 |
Prolonged bleeding time |
|
| C0151779 |
BXGD003473 |
Cutaneous Melanoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0151786 |
BXGD003475 |
Muscle Weakness |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases |
| C0151811 |
BXGD003478 |
Subcutaneous nodule |
Neoplasms; Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| C0151825 |
BXGD003481 |
Bone pain |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases |
| C0151878 |
BXGD003495 |
Prolonged QT interval |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0151888 |
BXGD003497 |
Hyporeflexia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0151940 |
BXGD003506 |
Hypocalcemic tetany |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases |
| C0152013 |
BXGD003516 |
Adenocarcinoma of lung (disorder) |
Neoplasms |
| C0152018 |
BXGD003518 |
Esophageal carcinoma |
Digestive System Diseases; Neoplasms |
| C0152441 |
BXGD003594 |
Madelung Deformity |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0152459 |
BXGD003600 |
Linear atrophy |
Pathological Conditions, Signs and Symptoms |
| C0154143 |
BXGD003704 |
Toxic multinodular goiter |
Endocrine System Diseases |
| C0155120 |
BXGD003774 |
Corneal Dystrophy, Band-Shaped |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0175693 |
BXGD004001 |
Russell-Silver syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0175754 |
BXGD004015 |
Agenesis of corpus callosum |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0178468 |
BXGD004029 |
Autoimmune thyroid disease |
Immune System Diseases; Endocrine System Diseases |
| C0178874 |
BXGD004037 |
Tumor Progression |
Pathological Conditions, Signs and Symptoms |
| C0201976 |
BXGD004063 |
Creatinine measurement, serum (procedure) |
|
| C0202239 |
BXGD004087 |
Uric acid measurement (procedure) |
|
| C0206640 |
BXGD004205 |
Ossifying Fibroma |
Neoplasms |
| C0206642 |
BXGD004207 |
Parosteal Osteosarcoma |
Neoplasms |
| C0206667 |
BXGD004228 |
Adrenal Cortical Adenoma |
Neoplasms; Endocrine System Diseases |
| C0206674 |
BXGD004232 |
Adenoma, Villous |
Neoplasms |
| C0206686 |
BXGD004241 |
Adrenocortical carcinoma |
Neoplasms; Endocrine System Diseases |
| C0206698 |
BXGD004248 |
Cholangiocarcinoma |
Neoplasms |
| C0206709 |
BXGD004257 |
Cystadenoma, Serous |
Neoplasms |
| C0206724 |
BXGD004269 |
Sex Cord-Stromal Tumor |
Neoplasms |
| C0206754 |
BXGD004289 |
Neuroendocrine Tumors |
Neoplasms |
| C0220659 |
BXGD004314 |
Acrodysostosis |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0220668 |
BXGD004317 |
Congenital contractural arachnodactyly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0221263 |
BXGD004427 |
Cafe-au-Lait Spots |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0221271 |
BXGD004431 |
Elastosis perforans serpiginosa |
Skin and Connective Tissue Diseases |
| C0221355 |
BXGD004447 |
Macrocephaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C0221357 |
BXGD004449 |
Brachydactyly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0221406 |
BXGD004459 |
Pituitary-dependent Cushing's disease |
Nervous System Diseases; Endocrine System Diseases |
| C0232943 |
BXGD004570 |
Intermenstrual heavy bleeding |
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications |
| C0234985 |
BXGD004708 |
Mental deterioration |
Mental Disorders |
| C0235659 |
BXGD004763 |
Reduced fetal movement |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications |
| C0235986 |
BXGD004799 |
Growth hormone excess |
Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases |
| C0236048 |
BXGD004807 |
Polyposis, Gastric |
Digestive System Diseases; Neoplasms |
| C0238463 |
BXGD004938 |
Papillary thyroid carcinoma |
Neoplasms; Endocrine System Diseases |
| C0239174 |
BXGD004969 |
Late tooth eruption |
|
| C0239479 |
BXGD004982 |
Round face |
|
| C0239594 |
BXGD004987 |
Short finger |
|
| C0241240 |
BXGD005089 |
Tall stature |
|
| C0242184 |
BXGD005140 |
Hypoxia |
Pathological Conditions, Signs and Symptoms |
| C0242216 |
BXGD005141 |
Biliary calculi |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0242292 |
BXGD005146 |
McCune-Albright Syndrome |
Musculoskeletal Diseases |
| C0259779 |
BXGD005218 |
Fibrous Dysplasia |
|
| C0262929 |
BXGD005269 |
Myxoma of the Endocardium |
Neoplasms |
| C0264009 |
BXGD005361 |
Osteodystrophy |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C0265329 |
BXGD005518 |
Organoid Nevus Phakomatosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases |
| C0265535 |
BXGD005544 |
Trigonocephaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0265593 |
BXGD005552 |
Brachymetacarpia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0266061 |
BXGD005618 |
Open Bite |
Stomatognathic Diseases |
| C0266153 |
BXGD005623 |
Ectopic gastric tissue |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0268398 |
BXGD005933 |
Familial lichen amyloidosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases |
| C0268436 |
BXGD005946 |
Pseudohypoaldosteronism, Type I |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0269011 |
BXGD006049 |
Increased size of penis |
Male Urogenital Diseases |
| C0271527 |
BXGD006208 |
Cryptogenic sexual precocity |
Endocrine System Diseases |
| C0271561 |
BXGD006213 |
Somatotropin deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases |
| C0271790 |
BXGD006259 |
Subclinical hypothyroidism |
Endocrine System Diseases |
| C0271862 |
BXGD006273 |
Idiopathic parathyroidism |
Endocrine System Diseases |
| C0272178 |
BXGD006316 |
Drug-induced neutropenia |
Hemic and Lymphatic Diseases |
| C0278510 |
BXGD006526 |
Childhood Medulloblastoma |
Neoplasms |
| C0278608 |
BXGD006549 |
Adult Liposarcoma |
Neoplasms |
| C0278701 |
BXGD006566 |
Gastric Adenocarcinoma |
Digestive System Diseases; Neoplasms |
| C0278704 |
BXGD006567 |
Malignant Childhood Neoplasm |
Neoplasms |
| C0278864 |
BXGD006604 |
Growth Hormone-Producing Pituitary Gland Neoplasm |
Neoplasms; Nervous System Diseases; Endocrine System Diseases |
| C0278876 |
BXGD006607 |
Adult Medulloblastoma |
Neoplasms |
| C0279702 |
BXGD006685 |
Conventional (Clear Cell) Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0279984 |
BXGD006703 |
Childhood Liposarcoma |
Neoplasms |
| C0280100 |
BXGD006713 |
Solid Neoplasm |
Neoplasms |
| C0280321 |
BXGD006739 |
Squamous cell carcinoma of the hypopharynx |
|
| C0281361 |
BXGD006774 |
Adenocarcinoma of pancreas |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0281952 |
BXGD006791 |
Pseudohypothyroidism |
Endocrine System Diseases |
| C0282160 |
BXGD006797 |
Aplasia Cutis Congenita |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0302840 |
BXGD006855 |
Toxic thyroid adenoma |
Neoplasms; Endocrine System Diseases |
| C0332563 |
BXGD006894 |
Papule |
Pathological Conditions, Signs and Symptoms |
| C0334041 |
BXGD006982 |
Osteoma cutis |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases |
| C0334307 |
BXGD007029 |
Tubulovillous adenoma |
Neoplasms |
| C0334569 |
BXGD007115 |
Odontogenic myxoma |
Neoplasms |
| C0338078 |
BXGD007166 |
Non-Functioning Pituitary Gland Neoplasm |
Neoplasms; Nervous System Diseases; Endocrine System Diseases |
| C0338656 |
BXGD007211 |
Impaired cognition |
Mental Disorders |
| C0339143 |
BXGD007226 |
Thyroid associated opthalmopathies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Immune System Diseases; Endocrine System Diseases |
| C0342198 |
BXGD007442 |
Thyrotoxicosis due to pituitary thyroid hormone resistance |
Endocrine System Diseases |
| C0342208 |
BXGD007445 |
Multinodular goiter |
Neoplasms; Endocrine System Diseases |
| C0342346 |
BXGD007467 |
Pseudohypoparathyroidism and pseudopseudohypoparathyroidism |
Nutritional and Metabolic Diseases; Endocrine System Diseases |
| C0342443 |
BXGD007481 |
Adrenal Cushing's syndrome |
Endocrine System Diseases |
| C0342494 |
BXGD007489 |
Adrenocortical hyperplasia |
Endocrine System Diseases |
| C0342495 |
BXGD007490 |
Macronodular adrenal hyperplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C0342543 |
BXGD007500 |
Central Precocious Puberty |
Endocrine System Diseases |
| C0342549 |
BXGD007504 |
Familial Testotoxicosis |
Endocrine System Diseases |
| C0343641 |
BXGD007636 |
Human papilloma virus infection |
Infections |
| C0345905 |
BXGD007746 |
Intrahepatic Cholangiocarcinoma |
Neoplasms |
| C0346302 |
BXGD007807 |
Growth Hormone-Secreting Pituitary Adenoma |
Neoplasms; Nervous System Diseases; Endocrine System Diseases |
| C0346429 |
BXGD007828 |
Multiple malignancy |
Neoplasms |
| C0346629 |
BXGD007831 |
Malignant neoplasm of large intestine |
Digestive System Diseases; Neoplasms |
| C0348801 |
BXGD007880 |
Group B streptococcal pneumonia |
Infections; Respiratory Tract Diseases |
| C0349588 |
BXGD007933 |
Short stature |
|
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0392525 |
BXGD008052 |
Nephrolithiasis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0399526 |
BXGD008251 |
Class III malocclusion |
Stomatognathic Diseases |
| C0403823 |
BXGD008315 |
Asthenozoospermia |
Male Urogenital Diseases |
| C0405578 |
BXGD008324 |
Gigantism and acromegaly |
Nervous System Diseases; Endocrine System Diseases |
| C0406810 |
BXGD008374 |
Carney Complex |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Cardiovascular Diseases |
| C0409959 |
BXGD008400 |
Osteoarthritis, Knee |
Musculoskeletal Diseases |
| C0410528 |
BXGD008430 |
Skeletal dysplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0423757 |
BXGD008504 |
Thin skin |
|
| C0423798 |
BXGD008510 |
Increased tendency to bruise |
Wounds and Injuries |
| C0424295 |
BXGD008524 |
Hyperactive behavior |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0428883 |
BXGD008639 |
Diastolic blood pressure |
|
| C0428886 |
BXGD008640 |
Mean blood pressure |
|
| C0432072 |
BXGD008718 |
Dysmorphic features |
|
| C0432123 |
BXGD008724 |
Sagittal craniosynostosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0456070 |
BXGD008863 |
Growth delay |
|
| C0456909 |
BXGD008883 |
Blindness |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0476073 |
BXGD008976 |
Papillary neoplasm |
Neoplasms |
| C0496779 |
BXGD009041 |
Malignant neoplasm of appendix |
Digestive System Diseases; Neoplasms |
| C0521525 |
BXGD009139 |
Short neck |
|
| C0524620 |
BXGD009236 |
Metabolic Syndrome X |
Nutritional and Metabolic Diseases |
| C0541794 |
BXGD009262 |
Skeletal muscle atrophy |
|
| C0544886 |
BXGD009319 |
Somatic mutation |
|
| C0546837 |
BXGD009343 |
Malignant neoplasm of esophagus |
Digestive System Diseases; Neoplasms |
| C0549473 |
BXGD009384 |
Thyroid carcinoma |
Neoplasms; Endocrine System Diseases |
| C0553665 |
BXGD009405 |
Skin endocrine disorder |
Skin and Connective Tissue Diseases |
| C0553694 |
BXGD009409 |
Oropharyngeal disorders |
Digestive System Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| C0555198 |
BXGD009432 |
Malignant Glioma |
Neoplasms |
| C0585442 |
BXGD009593 |
Osteosarcoma of bone |
Neoplasms |
| C0586358 |
BXGD009605 |
Biliary Intraepithelial Neoplasia |
Digestive System Diseases |
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C0677886 |
BXGD009734 |
Epithelial ovarian cancer |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0685938 |
BXGD009829 |
Malignant neoplasm of gastrointestinal tract |
Digestive System Diseases; Neoplasms |
| C0699790 |
BXGD009866 |
Colon Carcinoma |
Digestive System Diseases; Neoplasms |
| C0699791 |
BXGD009867 |
Stomach Carcinoma |
Digestive System Diseases; Neoplasms |
| C0699885 |
BXGD009869 |
Carcinoma of bladder |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0700095 |
BXGD009875 |
Central neuroblastoma |
Neoplasms; Nervous System Diseases |
| C0700292 |
BXGD009884 |
Hypoxemia |
Pathological Conditions, Signs and Symptoms |
| C0700502 |
BXGD009893 |
Acquired hypothyroidism |
Endocrine System Diseases |
| C0740394 |
BXGD009989 |
Hyperuricemia |
Pathological Conditions, Signs and Symptoms |
| C0740651 |
BXGD010004 |
Abdominal symptom |
|
| C0745106 |
BXGD010115 |
hyperparathyroid |
|
| C0750887 |
BXGD010240 |
Adrenal Cancer |
Neoplasms; Endocrine System Diseases |
| C0796000 |
BXGD010774 |
Multiple non-ossifying fibromatosis |
|
| C0853879 |
BXGD010982 |
Invasive carcinoma of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0855740 |
BXGD011086 |
Abnormal platelet function |
|
| C0857973 |
BXGD011167 |
Elevated circulating parathyroid hormone level |
|
| C0876973 |
BXGD011322 |
Infectious Lung Disorder |
Infections; Respiratory Tract Diseases |
| C0878659 |
BXGD011380 |
Disproportionate short stature |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0917816 |
BXGD011419 |
Mental deficiency |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0920184 |
BXGD011457 |
Fundic gland polyp |
Pathological Conditions, Signs and Symptoms |
| C0920563 |
BXGD011469 |
Insulin Sensitivity |
Nutritional and Metabolic Diseases |
| C0940937 |
BXGD011490 |
precancerous lesions |
|
| C0948008 |
BXGD011499 |
Ischemic stroke |
Nervous System Diseases; Cardiovascular Diseases |
| C0948187 |
BXGD011513 |
Tracheomalacia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Respiratory Tract Diseases |
| C0948896 |
BXGD011563 |
Primary hypogonadism |
Endocrine System Diseases |
| C1096155 |
BXGD011605 |
Macrophage Activation Syndrome |
Immune System Diseases |
| C1136382 |
BXGD011717 |
Sclerocystic Ovaries |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C1142276 |
BXGD011746 |
Renal anemia |
|
| C1168401 |
BXGD011792 |
Squamous cell carcinoma of the head and neck |
Neoplasms |
| C1257915 |
BXGD011813 |
Intestinal Polyposis |
Digestive System Diseases |
| C1261473 |
BXGD011855 |
Sarcoma |
Neoplasms |
| C1263023 |
BXGD011888 |
Macroorchidism |
|
| C1263846 |
BXGD011897 |
Attention deficit hyperactivity disorder |
Mental Disorders |
| C1266025 |
BXGD011935 |
Traditional Serrated Adenoma |
Neoplasms |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1298180 |
BXGD012246 |
Single tumor |
|
| C1302401 |
BXGD012303 |
Adenoma of large intestine |
Digestive System Diseases; Neoplasms |
| C1306050 |
BXGD012351 |
Primary malignant neoplasm of appendix |
Digestive System Diseases; Neoplasms |
| C1306214 |
BXGD012356 |
ACTH-Secreting Pituitary Adenoma |
Neoplasms; Nervous System Diseases; Endocrine System Diseases |
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1306710 |
BXGD012372 |
Facial asymmetry |
Pathological Conditions, Signs and Symptoms |
| C1319315 |
BXGD012415 |
Adenocarcinoma of large intestine |
Digestive System Diseases; Neoplasms |
| C1332243 |
BXGD012516 |
Adenocarcinoma of ampulla of Vater |
Neoplasms |
| C1332986 |
BXGD012574 |
Childhood Osteosarcoma |
Neoplasms |
| C1333119 |
BXGD012600 |
Colorectal Villous Adenoma |
Neoplasms |
| C1334260 |
BXGD012690 |
Intramuscular Myxoma |
Neoplasms |
| C1334274 |
BXGD012695 |
Invasive Carcinoma |
Neoplasms |
| C1335302 |
BXGD012775 |
Pancreatic Ductal Adenocarcinoma |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C1367554 |
BXGD012885 |
Adamantinoma |
Neoplasms; Musculoskeletal Diseases |
| C1384514 |
BXGD012940 |
Conn Syndrome |
Endocrine System Diseases |
| C1384666 |
BXGD012948 |
hearing impairment |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C1386048 |
BXGD012950 |
Intrauterine retardation |
|
| C1389280 |
BXGD012967 |
Basal ganglia calcification |
|
| C1449842 |
BXGD013093 |
Pseudohypoaldosteronism, Type I, Autosomal Dominant |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1449843 |
BXGD013094 |
Pseudohypoaldosteronism, Type I, Autosomal Recessive |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1449844 |
BXGD013095 |
Pseudohypoaldosteronism, Type II |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1458155 |
BXGD013136 |
Mammary Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C1504412 |
BXGD013143 |
Testotoxicosis |
Endocrine System Diseases |
| C1519176 |
BXGD013232 |
Salivary Gland Pleomorphic Adenoma |
Neoplasms; Stomatognathic Diseases |
| C1519353 |
BXGD013236 |
Skin Papule |
Skin and Connective Tissue Diseases |
| C1527349 |
BXGD013277 |
Ductal Breast Carcinoma |
Neoplasms |
| C1561643 |
BXGD013363 |
Chronic Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1561826 |
BXGD013364 |
Overweight and obesity |
|
| C1608408 |
BXGD013434 |
Malignant transformation |
|
| C1611743 |
BXGD013456 |
Familial (FPAH) |
|
| C1621958 |
BXGD013468 |
Glioblastoma Multiforme |
Neoplasms |
| C1707332 |
BXGD013581 |
Cellular Myxoma |
|
| C1708747 |
BXGD013609 |
Low grade appendiceal mucinous neoplasm |
|
| C1709353 |
BXGD013624 |
Osteofibrous Dysplasia |
Musculoskeletal Diseases |
| C1709780 |
BXGD013632 |
Pyloric Gland Adenoma |
|
| C1710140 |
BXGD013640 |
Sparsely Granulated Somatotroph Adenoma |
Neoplasms; Nervous System Diseases; Endocrine System Diseases |
| C1739135 |
BXGD013733 |
Progression of prostate cancer |
|
| C1740827 |
BXGD013746 |
CLL progression |
|
| C1832661 |
BXGD013866 |
ANOPHTHALMIA AND PULMONARY HYPOPLASIA |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases |
| C1836195 |
BXGD014094 |
Short toe |
|
| C1836438 |
BXGD014114 |
Familial neurocardiogenic syncope |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1836542 |
BXGD014129 |
Depressed nasal bridge |
|
| C1837084 |
BXGD014195 |
Short metacarpal |
|
| C1837142 |
BXGD014201 |
Poor suck |
|
| C1837315 |
BXGD014218 |
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 |
|
| C1840309 |
BXGD014444 |
Short 4th metacarpal |
|
| C1842774 |
BXGD014536 |
Hypermelanotic macule |
|
| C1843366 |
BXGD014575 |
NIEMANN-PICK DISEASE, TYPE C2 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases |
| C1843367 |
BXGD014576 |
Poor school performance |
|
| C1844548 |
BXGD014642 |
Hypoplastic finger |
|
| C1848701 |
BXGD014967 |
Elevated hepatic transaminase |
|
| C1849020 |
BXGD014996 |
Short metatarsal |
|
| C1849211 |
BXGD015023 |
Generalized hirsutism |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C1849265 |
BXGD015028 |
Overgrowth |
|
| C1850631 |
BXGD015163 |
Short 3rd metacarpal |
|
| C1851833 |
BXGD015240 |
Premature birth following premature rupture of fetal membranes |
Female Urogenital Diseases and Pregnancy Complications |
| C1853237 |
BXGD015319 |
Isolated cases |
|
| C1855841 |
BXGD015550 |
Hypocalcemic seizures |
Nutritional and Metabolic Diseases |
| C1857108 |
BXGD015677 |
Limitation of joint mobility |
|
| C1857276 |
BXGD015688 |
Trichohepatoenteric Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases |
| C1857451 |
BXGD015702 |
Acth-Independent Macronodular Adrenal Hyperplasia |
Endocrine System Diseases |
| C1858452 |
BXGD015796 |
Thickened calvaria |
|
| C1860819 |
BXGD016002 |
Metopic synostosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C1861305 |
BXGD016027 |
TARSAL-CARPAL COALITION SYNDROME |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C1861388 |
BXGD016044 |
Short 5th metacarpal |
|
| C1861403 |
BXGD016045 |
Variable expressivity |
|
| C1861975 |
BXGD016095 |
Cafe au lait spots, multiple |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C1863184 |
BXGD016153 |
Choroid plexus calcification |
|
| C1863402 |
BXGD016174 |
Broad distal phalanx of the thumb |
|
| C1864100 |
BXGD016212 |
PSEUDOHYPOPARATHYROIDISM, TYPE IB |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C1864105 |
BXGD016213 |
Low urinary cyclic AMP response to PTH administration |
|
| C1866231 |
BXGD016388 |
Full cheeks |
|
| C1868085 |
BXGD016486 |
Craniofacial hyperostosis |
|
| C1868394 |
BXGD016499 |
Elevated calcitonin |
|
| C1868683 |
BXGD016526 |
B-CELL MALIGNANCY, LOW-GRADE |
|
| C1868684 |
BXGD016527 |
EAR, PATELLA, SHORT STATURE SYNDROME |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases |
| C1963060 |
BXGD016679 |
Agitation, CTCAE 3.0 |
|
| C1963077 |
BXGD016680 |
Bone Pain, CTCAE 3.0 |
|
| C1963184 |
BXGD016688 |
Nystagmus, CTCAE 3.0 |
|
| C1963946 |
BXGD016707 |
Laryngeal dystonia |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases |
| C2062372 |
BXGD016895 |
Adrenal hyperplasia, bilateral |
|
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2674432 |
BXGD017246 |
Reduced bone mineral density |
|
| C2675383 |
BXGD017286 |
POLYOSTOTIC FIBROUS DYSPLASIA, SOMATIC, MOSAIC |
|
| C2675481 |
BXGD017292 |
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 |
|
| C2677123 |
BXGD017364 |
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 |
|
| C2700617 |
BXGD017474 |
Irritation - emotion |
Behavior and Behavior Mechanisms |
| C2713447 |
BXGD017501 |
Hyperpotassemia and Hypertension, Familial |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C2919142 |
BXGD017867 |
Short Stature, CTCAE |
|
| C2930619 |
BXGD017890 |
Sex Differentiation Disorders |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C2931404 |
BXGD018018 |
Albright's hereditary osteodystrophy |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C2932715 |
BXGD018100 |
Pseudohypoparathyroidism Type 1B |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C2932716 |
BXGD018101 |
Pseudohypoparathyroidism Type 1C |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C2940785 |
BXGD018183 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C2940786 |
BXGD018184 |
Thyroid Hormone Resistance Syndrome |
Endocrine System Diseases |
| C3160815 |
BXGD018478 |
Intraductal papillary mucinous neoplasm |
|
| C3463824 |
BXGD018899 |
MYELODYSPLASTIC SYNDROME |
Hemic and Lymphatic Diseases |
| C3489630 |
BXGD018939 |
Somatotrophinoma, Familial |
Neoplasms; Nervous System Diseases; Endocrine System Diseases |
| C3493776 |
BXGD018955 |
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C3494506 |
BXGD018968 |
Pseudohypoparathyroidism, Type Ia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C3536983 |
BXGD019078 |
Familial Hypophosphatemic Rickets |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital Diseases |
| C3548479 |
BXGD019120 |
response to bronchodilator |
|
| C3554460 |
BXGD019215 |
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 |
|
| C3697137 |
BXGD019353 |
Fibrous dysplasia of bone with intramuscular myxoma |
Musculoskeletal Diseases |
| C3714524 |
BXGD019410 |
Fibromyxosarcoma |
Neoplasms |
| C3714756 |
BXGD019429 |
Intellectual Disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C3714796 |
BXGD019434 |
Isolated somatotropin deficiency |
|
| C3805278 |
BXGD019474 |
Extrahepatic Cholangiocarcinoma |
Neoplasms |
| C3805574 |
BXGD019481 |
Increased fracture rate |
|
| C3806226 |
BXGD019502 |
Ectopic calcification |
|
| C3806442 |
BXGD019510 |
Myoclonic spasms |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C3828530 |
BXGD019744 |
Platelet Component Distribution Width Measurement |
|
| C3887650 |
BXGD019911 |
Adult Rickets |
Nutritional and Metabolic Diseases; Musculoskeletal Diseases |
| C3887896 |
BXGD019925 |
Primary Adrenal Insufficiency |
|
| C4014803 |
BXGD020167 |
ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2 |
|
| C4016140 |
BXGD020278 |
PSEUDOHYPOPARATHYROIDISM, TYPE IA, WITH TESTOTOXICOSIS |
|
| C4021649 |
BXGD020719 |
Short fifth metatarsal |
|
| C4021745 |
BXGD020752 |
Abnormality of the musculature |
|
| C4021790 |
BXGD020782 |
Abnormality of the skeletal system |
|
| C4021800 |
BXGD020790 |
Abnormality of dental enamel |
|
| C4021815 |
BXGD020801 |
Abnormal palate morphology |
|
| C4023009 |
BXGD021062 |
Constrictive median neuropathy |
Nervous System Diseases |
| C4023096 |
BXGD021104 |
Ectopic ossification in muscle tissue |
Pathological Conditions, Signs and Symptoms |
| C4023681 |
BXGD021239 |
Delayed fine motor development |
|
| C4024097 |
BXGD021287 |
Broad 1st metacarpal |
|
| C4024878 |
BXGD021453 |
Generalized hyperpigmentation |
Skin and Connective Tissue Diseases |
| C4025151 |
BXGD021568 |
Increased bone density with cystic changes |
Musculoskeletal Diseases |
| C4025174 |
BXGD021575 |
Large cafe-au-lait macules with irregular margins |
|
| C4025515 |
BXGD021663 |
Cortical subperiosteal resorption of humeral metaphyses |
|
| C4025651 |
BXGD021712 |
Increased circulating cortisol level |
|
| C4025669 |
BXGD021720 |
Decreased circulating ACTH level |
|
| C4025760 |
BXGD021781 |
Primary hypercortisolism |
|
| C4025822 |
BXGD021810 |
Abnormality of the parathyroid gland |
|
| C4025846 |
BXGD021826 |
Abnormality of vision |
|
| C4025860 |
BXGD021833 |
Hearing abnormality |
|
| C4072940 |
BXGD022026 |
Ossifying fibroma of the jaw |
Neoplasms; Stomatognathic Diseases |
| C4086165 |
BXGD022126 |
Childhood Neuroblastoma |
Neoplasms |
| C4281993 |
BXGD022418 |
Neonatal respiratory distress |
Respiratory Tract Diseases |
| C4284013 |
BXGD022428 |
Primary cholangiocarcinoma of intrahepatic biliary tract |
Neoplasms |
| C4304832 |
BXGD022585 |
Primary pigmented nodular adrenocortical disease |
|
| C4316995 |
BXGD022715 |
Primary Hypothyroidism |
Endocrine System Diseases |
| C4511687 |
BXGD023010 |
Pancreatic Intraductal Papillary Mucinous Neoplasm |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C4540135 |
BXGD023240 |
PITUITARY ADENOMA 3, MULTIPLE TYPES |
|
| C4540536 |
BXGD023269 |
PITUITARY TUMOR 3, GROWTH HORMONE-SECRETING, SOMATIC |
|
| C4551560 |
BXGD023349 |
Truncal obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C4551683 |
BXGD023389 |
Adrenal Gland Pheochromocytoma |
Neoplasms; Endocrine System Diseases |
| C4551686 |
BXGD023391 |
Malignant neoplasm of soft tissue |
Neoplasms |
| C4551853 |
BXGD023421 |
Diaphyseal sclerosis |
|
| C4552810 |
BXGD023525 |
Irritability, CTCAE |
|
| C4552855 |
BXGD023528 |
Agitation, CTCAE 5.0 |
|
| C4554036 |
BXGD023557 |
Nystagmus, CTCAE 5.0 |
|
| C4554063 |
BXGD023559 |
Bone Pain, CTCAE 5.0 |
|
| C4721610 |
BXGD023760 |
Carcinoma, Ovarian Epithelial |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases |
| C4722085 |
BXGD023788 |
Malignant neoplasm of colon and/or rectum |
|
| C4722330 |
BXGD023801 |
Generalized Thyroid Hormone Resistance |
Endocrine System Diseases |
| C4727687 |
BXGD023871 |
Advanced Laryngeal Squamous Cell Carcinoma |
|
| C4732730 |
BXGD023895 |
Blood spots |
|