| 1 | Sickle Cell Trait | 46.2% |
| 2 | Thalassemia | 38.2% |
| 3 | Respiratory Distress Syndrome, Adult | 27% |
| 4 | Respiratory Distress Syndrome, Newborn | 26.2% |
| 5 | Cystic Fibrosis | 24.6% |
| 6 | Meconium Aspiration Syndrome | 23.4% |
| 7 | Bronchitis, Chronic | 21.1% |
| 8 | Bronchitis | 21% |
| 9 | Pneumonia | 20.3% |
| 10 | Lobar Pneumonia | 20.3% |
| 11 | Pneumonitis | 20.3% |
| 12 | Pleuropneumonia | 20% |
| 13 | Thrombasthenia | 19.6% |
| 14 | Antithrombin III Deficiency | 19.6% |
| 15 | Protein C Deficiency | 19.6% |
| 16 | Bronchopneumonia | 19.3% |
| 17 | Pelger-Huet Anomaly | 19.2% |
| 18 | Hyaline Membrane Disease | 19.1% |
| 19 | Kartagener Syndrome | 18.9% |
| 20 | Asthma | 18.8% |
| 21 | Wiskott-Aldrich Syndrome | 18.8% |
| 22 | Tracheobronchomegaly | 18.3% |
| 23 | Idiopathic Pulmonary Fibrosis | 18.2% |
| 24 | Lung Diseases, Fungal | 18.1% |
| 25 | Pneumoconiosis | 18.1% |
| 26 | Vocal Cord Dysfunction | 18.1% |
| 27 | Lung Abscess | 17.9% |
| 28 | Lung Neoplasms | 17.9% |
| 29 | Tuberculosis, Pulmonary | 17.9% |
| 30 | Afibrinogenemia | 17.6% |
| 31 | Factor VII Deficiency | 17.6% |
| 32 | Factor X Deficiency | 17.6% |
| 33 | Factor XII Deficiency | 17.6% |
| 34 | Hemophilia A | 17.6% |
| 35 | Activated Protein C Resistance | 17.6% |
| 36 | Factor II deficiency | 17.6% |
| 37 | Factor VIII Deficiency | 17.6% |
| 38 | Factor V deficiency | 17.6% |
| 39 | Factor XI Deficiency | 17.6% |
| 40 | Hypoprothrombinemias | 17.6% |
| 41 | Disseminated Intravascular Coagulation | 17.5% |
| 42 | Protein S Deficiency | 17.5% |
| 43 | Granuloma, Laryngeal | 17.2% |
| 44 | Scimitar Syndrome | 16.3% |
| 45 | Bronchiolitis | 16.2% |
| 46 | Anemia, Diamond-Blackfan | 16.2% |
| 47 | Pulmonary Eosinophilia | 16.1% |
| 48 | Eosinophilic Pneumonia | 16.1% |
| 49 | Radiation Pneumonitis | 16% |
| 50 | Radiation Fibrosis | 16% |
| 51 | Primary Ciliary Dyskinesia | 15.9% |
| 52 | Thrombocythemia, Essential | 15.8% |
| 53 | Altitude Sickness | 15.3% |
| 54 | Atelectasis | 15.3% |
| 55 | Pulmonary Hypertension | 15.3% |
| 56 | Pulmonary Alveolar Proteinosis | 15.3% |
| 57 | Pulmonary Edema | 15.3% |
| 58 | Pulmonary Fibrosis | 15.3% |
| 59 | Respiratory Insufficiency | 15.3% |
| 60 | Hamman-Rich syndrome | 15.3% |
| 61 | Lung Diseases, Interstitial | 15.3% |
| 62 | Respiratory Depression | 15.3% |
| 63 | Lung Diseases, Obstructive | 15.3% |
| 64 | Respiratory Failure | 15.3% |
| 65 | Aspiration Pneumonia | 15% |
| 66 | Asbestosis | 14.8% |
| 67 | Berylliosis | 14.8% |
| 68 | Silicosis | 14.8% |
| 69 | Anemia, Neonatal | 14.6% |
| 70 | Aspergillosis, Allergic Bronchopulmonary | 14.5% |
| 71 | Persistent Fetal Circulation Syndrome | 14.2% |
| 72 | Hemoglobinuria, Paroxysmal | 14.2% |
| 73 | Aicardi's syndrome | 14% |
| 74 | Pneumonia, Viral | 13.6% |
| 75 | Pleurisy | 13.5% |
| 76 | Tracheitis | 13.5% |
| 77 | Lung Injury | 13.5% |
| 78 | Hepatopulmonary Syndrome | 13.5% |
| 79 | Respiratory Aspiration | 13.5% |
| 80 | Apnea | 13.4% |
| 81 | Cheyne-Stokes Respiration | 13.4% |
| 82 | Dyspnea | 13.4% |
| 83 | Hyperventilation | 13.4% |
| 84 | Mouth Breathing | 13.4% |
| 85 | Tachypnea | 13.4% |
| 86 | Pneumonia, Bacterial | 13.4% |
| 87 | CHARGE Syndrome | 13.4% |
| 88 | Pulmonary Embolism | 13.3% |
| 89 | Laryngospasm | 13.3% |
| 90 | Blood Coagulation Disorders | 13.3% |
| 91 | Blood Platelet Disorders | 13.3% |
| 92 | Bone Marrow Diseases | 13.3% |
| 93 | Hemorrhagic Disorders | 13.3% |
| 94 | Leukocyte Disorders | 13.3% |
| 95 | Methemoglobinemia | 13.3% |
| 96 | Pancytopenia | 13.3% |
| 97 | Polycythemia | 13.3% |
| 98 | Sulfhemoglobinemia | 13.3% |
| 99 | Thrombophilia | 13.3% |
| 100 | Erythrocytosis | 13.3% |
| 101 | Transfusion-Related Acute Lung Injury | 13.3% |
| 102 | Multiple Pulmonary Nodules | 13.2% |
| 103 | Choanal Atresia | 12.9% |
| 104 | Laryngocele | 12.9% |
| 105 | Neoplastic Syndromes, Hereditary | 12.9% |
| 106 | Ichthyosis, X-Linked | 12.7% |
| 107 | Hydrops Fetalis | 12.6% |
| 108 | Multiple Epiphyseal Dysplasia | 12.6% |
| 109 | Osteochondrodysplasias | 12.6% |
| 110 | Werner Syndrome | 12.6% |
| 111 | Myasthenic Syndromes, Congenital | 12.6% |
| 112 | Pneumonia, Lipid | 12.4% |
| 113 | Albinism | 12.3% |
| 114 | Hoarseness | 12.2% |
| 115 | Histiocytosis, Langerhans-Cell | 12.1% |
| 116 | Nail-Patella Syndrome | 12.1% |
| 117 | Laryngitis | 12.1% |
| 118 | Rhinitis | 12.1% |
| 119 | Bronchial Fistula | 12% |
| 120 | Pleural Neoplasms | 12% |
| 121 | Transfusion Reaction | 11.9% |
| 122 | Hypotensive Transfusion Reaction | 11.9% |
| 123 | Pleural Effusion, Malignant | 11.9% |
| 124 | Hemoptysis | 11.9% |
| 125 | Fragile X Syndrome | 11.9% |
| 126 | Autoimmune Lymphoproliferative Syndrome | 11.9% |
| 127 | Muscular Dystrophy, Duchenne | 11.9% |
| 128 | Anemia, Macrocytic | 11.7% |
| 129 | Bronchial Diseases | 11.7% |
| 130 | Pleural Diseases | 11.7% |
| 131 | Thoracic Diseases | 11.7% |
| 132 | Tracheal Diseases | 11.7% |
| 133 | Pregnancy Complications, Hematologic | 11.7% |
| 134 | Hematologic Neoplasms | 11.7% |
| 135 | Bone Marrow Neoplasms | 11.6% |
| 136 | Cockayne Syndrome | 11.6% |
| 137 | Vitamin K Deficiency | 11.6% |
| 138 | Bronchiolitis Obliterans | 11.5% |
| 139 | Dwarfism | 11.4% |
| 140 | Airway Obstruction | 11.4% |
| 141 | Choking | 11.4% |
| 142 | Chronic Obstructive Airway Disease | 11.4% |
| 143 | Middle Lobe Syndrome | 11.4% |
| 144 | Acute Lung Injury | 11.4% |
| 145 | Fanconi Anemia | 11.4% |
| 146 | Sarcoidosis, Pulmonary | 11.3% |
| 147 | Muscular Dystrophy | 11.1% |
| 148 | Osteogenesis Imperfecta | 11.1% |
| 149 | Beckwith-Wiedemann Syndrome | 11.1% |
| 150 | Wolf-Hirschhorn Syndrome | 11.1% |
| 151 | Alstrom Syndrome | 10.9% |
| 152 | Bronchopulmonary Dysplasia | 10.8% |
| 153 | Tracheal Neoplasms | 10.7% |
| 154 | Farmer's Lung | 10.6% |
| 155 | Thrombocytosis | 10.5% |
| 156 | Laryngeal Diseases | 10.5% |
| 157 | Nose Diseases | 10.5% |
| 158 | Sinusitis | 10.4% |
| 159 | Bronchial Neoplasms | 10.4% |
| 160 | Marfan Syndrome | 10.3% |
| 161 | Respiratory Tract Infections | 10.3% |
| 162 | Hemolytic-Uremic Syndrome | 10.3% |
| 163 | Granuloma, Respiratory Tract | 10.2% |
| 164 | Respiratory Hypersensitivity | 10.2% |
| 165 | Respiratory Tract Fistula | 10.2% |
| 166 | Chronic granulomatous disease | 10.2% |
| 167 | Smith-Magenis syndrome | 10% |
| 168 | Pulmonary Aspergillosis | 10% |
| 169 | Bronchopulmonary Aspergillosis | 10% |
| 170 | Hypoventilation | 10% |
| 171 | Eosinophilic Granuloma | 9.9% |
| 172 | Cri-du-Chat Syndrome | 9.9% |
| 173 | Down Syndrome | 9.9% |
| 174 | Angioedemas, Hereditary | 9.9% |
| 175 | Trisomy 21 | 9.9% |
| 176 | Acidosis, Respiratory | 9.9% |
| 177 | Alkalosis, Respiratory | 9.9% |
| 178 | Sleep Apnea Syndromes | 9.9% |
| 179 | Blastomycosis | 9.9% |
| 180 | Pulmonary Infarction | 9.9% |
| 181 | Laryngeal neoplasm | 9.9% |
| 182 | Acute Chest Syndrome | 9.8% |
| 183 | Menkes Kinky Hair Syndrome | 9.8% |
| 184 | Mucopolysaccharidosis II | 9.7% |
| 185 | Anemia, Sickle Cell | 9.7% |
| 186 | Holoprosencephaly | 9.7% |
| 187 | Polycythemia Vera | 9.6% |
| 188 | Pulmonary Emphysema | 9.4% |
| 189 | Paranasal Sinus Neoplasms | 9.2% |
| 190 | Myotonic Dystrophy | 9.1% |
| 191 | Kallmann Syndrome | 9.1% |
| 192 | Ectodermal Dysplasia | 9.1% |
| 193 | Aplasia Cutis Congenita | 9.1% |
| 194 | Prader-Willi Syndrome | 9% |
| 195 | Dyspnea, Paroxysmal | 8.8% |
| 196 | Respiratory Paralysis | 8.8% |
| 197 | Asthma, Exercise-Induced | 8.8% |
| 198 | Status Asthmaticus | 8.8% |
| 199 | Granulomatosis with polyangiitis | 8.8% |
| 200 | Deformity | 8.8% |
| 201 | Tuberous Sclerosis | 8.8% |
| 202 | Rett Syndrome | 8.8% |
| 203 | Pseudoxanthoma Elasticum | 8.7% |
| 204 | Rubinstein-Taybi Syndrome | 8.6% |
| 205 | Familial Mediterranean Fever | 8.5% |
| 206 | Lymphatic Diseases | 8.4% |
| 207 | Adrenoleukodystrophy | 8.4% |
| 208 | Nose Neoplasms | 8.3% |
| 209 | Laryngostenosis | 8.2% |
| 210 | Rhinoscleroma | 8.2% |
| 211 | Purpura, Thrombotic Thrombocytopenic | 8.2% |
| 212 | Sleep Apnea, Obstructive | 8.2% |
| 213 | Sleep Apnea, Central | 8.2% |
| 214 | Smith-Lemli-Opitz Syndrome | 8.2% |
| 215 | Hepatolenticular Degeneration | 8.1% |
| 216 | Lymphatic Abnormalities | 8.1% |
| 217 | Asthma, Occupational | 8.1% |
| 218 | Sjogren-Larsson Syndrome | 8.1% |
| 219 | Neuronal Ceroid-Lipofuscinoses | 8.1% |
| 220 | Leukemoid Reaction | 8% |
| 221 | Anti-Glomerular Basement Membrane Disease | 7.9% |
| 222 | Polycystic Kidney Diseases | 7.9% |
| 223 | Williams Syndrome | 7.9% |
| 224 | Agammaglobulinemia | 7.8% |
| 225 | Fetal Diseases | 7.7% |
| 226 | Ataxia Telangiectasia | 7.7% |
| 227 | Refsum Disease | 7.7% |
| 228 | Bronchospasm | 7.7% |
| 229 | Bronchiectasis | 7.7% |
| 230 | Chylothorax | 7.7% |
| 231 | Hydropneumothorax | 7.7% |
| 232 | Hydrothorax | 7.7% |
| 233 | Pneumothorax | 7.7% |
| 234 | Tracheal Stenosis | 7.7% |
| 235 | Bronchial Hyperreactivity | 7.7% |
| 236 | Amyloid Neuropathies, Familial | 7.6% |
| 237 | Maxillary Sinus Neoplasms | 7.5% |
| 238 | Amino Acid Metabolism, Inborn Errors | 7.5% |
| 239 | Carbohydrate Metabolism, Inborn Errors | 7.5% |
| 240 | Metal Metabolism, Inborn Errors | 7.5% |
| 241 | Progeria | 7.5% |
| 242 | Lysosomal Storage Diseases | 7.5% |
| 243 | Cytochrome-c Oxidase Deficiency | 7.5% |
| 244 | Peroxisomal Disorders | 7.5% |
| 245 | Eosinophilia | 7.5% |
| 246 | Hypoproteinemia | 7.5% |
| 247 | Leukopenia | 7.5% |
| 248 | Thrombocytopenia | 7.5% |
| 249 | Leukostasis | 7.5% |
| 250 | MYELODYSPLASTIC SYNDROME | 7.5% |
| 251 | Retinal Dysplasia | 7.4% |
| 252 | Aniridia | 7.3% |
| 253 | Invasive Pulmonary Aspergillosis | 7.3% |
| 254 | Epidermolysis Bullosa | 7.3% |
| 255 | Asthma, Aspirin-Induced | 7.3% |
| 256 | Fabry Disease | 7.2% |
| 257 | Hay fever | 7.2% |
| 258 | Rhinitis, Allergic, Perennial | 7.2% |
| 259 | Anemia | 7.2% |
| 260 | Autoimmune thrombocytopenia | 7.1% |
| 261 | Immune thrombocytopenic purpura | 7.1% |
| 262 | Anemia, Megaloblastic | 7% |
| 263 | Infectious Mononucleosis | 7% |
| 264 | Atypical Hemolytic Uremic Syndrome | 6.8% |
| 265 | Waldenstrom Macroglobulinemia | 6.8% |
| 266 | Laryngomalacia | 6.8% |
| 267 | Granuloma, Lethal Midline | 6.8% |
| 268 | Laryngeal Edema | 6.8% |
| 269 | Nose Deformities, Acquired | 6.8% |
| 270 | Common Cold | 6.7% |
| 271 | Hemothorax | 6.7% |
| 272 | Influenza | 6.7% |
| 273 | Catarrh | 6.7% |
| 274 | Cutis Laxa | 6.7% |
| 275 | Retinitis Pigmentosa | 6.7% |
| 276 | Pigmentary retinopathy | 6.7% |
| 277 | Severe Acute Respiratory Syndrome | 6.7% |
| 278 | Laryngopharyngeal Reflux | 6.7% |
| 279 | Porokeratosis | 6.6% |
| 280 | Keratoderma, Palmoplantar | 6.6% |
| 281 | Leukocytosis | 6.6% |
| 282 | Paraproteinemias | 6.6% |
| 283 | Pleocytosis | 6.6% |
| 284 | Welander Distal Myopathy | 6.6% |
| 285 | Galactosemias | 6.5% |
| 286 | Urea Cycle Disorders, Inborn | 6.5% |
| 287 | Tyrosinemias | 6.5% |
| 288 | Cryoglobulinemia | 6.4% |
| 289 | Monoclonal Gammopathy of Undetermined Significance | 6.4% |
| 290 | Canavan Disease | 6.3% |
| 291 | Alexander Disease | 6.3% |
| 292 | Glycogen storage disease type II | 6.2% |
| 293 | Zellweger Syndrome | 6.2% |
| 294 | Lymphangiectasis, Intestinal | 6.1% |
| 295 | Duane Retraction Syndrome | 6.1% |
| 296 | Optic Atrophy, Hereditary, Leber | 6.1% |
| 297 | Kernicterus | 6% |
| 298 | Pharyngitis | 6% |
| 299 | Hyperphosphaturia | 6% |
| 300 | Porphyrias, Hepatic | 6% |
| 301 | Nasal Polyps | 6% |
| 302 | Peutz-Jeghers Syndrome | 6% |
| 303 | Myotonia Congenita | 6% |
| 304 | Brain Diseases, Metabolic, Inborn | 6% |
| 305 | Dystonia Musculorum Deformans | 5.9% |
| 306 | Pertussis | 5.9% |
| 307 | Lafora Disease | 5.9% |
| 308 | Unverricht-Lundborg Syndrome | 5.9% |
| 309 | Hypergammaglobulinemia | 5.9% |
| 310 | Lung diseases | 5.9% |
| 311 | Respiration Disorders | 5.9% |
| 312 | Purpura, Hyperglobulinemic | 5.8% |
| 313 | Ecchymosis | 5.8% |
| 314 | Petechiae | 5.8% |
| 315 | Purpura | 5.8% |
| 316 | Xeroderma Pigmentosum | 5.7% |
| 317 | Epiglottitis | 5.7% |
| 318 | Mediastinitis | 5.7% |
| 319 | Multiple Endocrine Neoplasia | 5.5% |
| 320 | Waterhouse-Friderichsen Syndrome | 5.5% |
| 321 | Heavy Chain Disease | 5.5% |
| 322 | Congenital Hypothyroidism | 5.5% |
| 323 | Dermatitis, Atopic | 5.4% |
| 324 | Voice Disorders | 5.4% |
| 325 | Voice Disturbance | 5.4% |
| 326 | Epistaxis | 5.4% |
| 327 | Multiple Myeloma | 5.4% |
| 328 | Xeroderma | 5.4% |
| 329 | Mobius Syndrome | 5.4% |
| 330 | Mucopolysaccharidosis III | 5.3% |
| 331 | Homocystinuria | 5.3% |
| 332 | Bronchomalacia | 5.3% |
| 333 | Tracheomalacia | 5.3% |
| 334 | Leigh Disease | 5.3% |
| 335 | Basal Cell Nevus Syndrome | 5.3% |
| 336 | Polycystic Kidney, Autosomal Dominant | 5.2% |
| 337 | POEMS Syndrome | 5.2% |
| 338 | Classical Lissencephalies and Subcortical Band Heterotopias | 5.2% |
| 339 | Hyperkeratosis, Epidermolytic | 5.2% |
| 340 | Mediastinal Cyst | 5% |
| 341 | Pericardial Cyst | 5% |
| 342 | Thymic Cyst | 5% |
| 343 | Thrombocytopenic purpura | 5% |
| 344 | Croup | 5% |
| 345 | Mediastinal Emphysema | 5% |
| 346 | Rhinitis, Vasomotor | 5% |
| 347 | Behcet Syndrome | 5% |
| 348 | Alkaptonuria | 4.9% |
| 349 | Glycogen Storage Disease | 4.9% |
| 350 | Hypophosphatasia | 4.9% |
| 351 | Propionic acidemia | 4.9% |
| 352 | Dihydropyrimidine Dehydrogenase Deficiency | 4.9% |
| 353 | Cystinosis | 4.9% |
| 354 | Vocal Cord Paralysis | 4.9% |
| 355 | Gaucher Disease | 4.8% |
| 356 | Abdominal Cramps | 4.8% |
| 357 | Abnormalities, Drug-Induced | 4.8% |
| 358 | Amniotic Band Syndrome | 4.8% |
| 359 | Asphyxia Neonatorum | 4.8% |
| 360 | Infant, Premature, Diseases | 4.8% |
| 361 | Situs Inversus | 4.8% |
| 362 | Infantile Colic | 4.8% |
| 363 | Charcot-Marie-Tooth Disease | 4.8% |
| 364 | Antley-Bixler Syndrome Phenotype | 4.8% |
| 365 | Primary Myelofibrosis | 4.6% |
| 366 | Agranulocytosis | 4.6% |
| 367 | Lymphocytosis | 4.6% |
| 368 | Myelofibrosis | 4.6% |
| 369 | Myeloid Metaplasia | 4.6% |
| 370 | Hypoalbuminemia | 4.6% |
| 371 | Hypereosinophilic syndrome | 4.6% |
| 372 | bone marrow fibrosis | 4.6% |
| 373 | Thrombotic Microangiopathies | 4.6% |
| 374 | Huntington Disease | 4.6% |
| 375 | Niemann-Pick Disease, Type C | 4.5% |
| 376 | Carbamoyl-Phosphate Synthase I Deficiency Disease | 4.5% |
| 377 | Tonsillitis | 4.4% |
| 378 | Adenitis | 4.4% |
| 379 | Histiocytosis | 4.4% |
| 380 | Lymphadenitis | 4.4% |
| 381 | Lymphangitis | 4.4% |
| 382 | Lymphedema | 4.4% |
| 383 | Splenic Diseases | 4.4% |
| 384 | Thymus Hyperplasia | 4.4% |
| 385 | Pseudolymphoma | 4.4% |
| 386 | Lymphadenopathy | 4.4% |
| 387 | Hypolipoproteinemias | 4.4% |
| 388 | Papillon-Lefevre Disease | 4.4% |
| 389 | Hyperlipidemia, Familial Combined | 4.4% |
| 390 | Hyperlipoproteinemia Type III | 4.4% |
| 391 | Eye Abnormalities | 4.3% |
| 392 | Cardiovascular Abnormalities | 4.3% |
| 393 | Anemia, Hemolytic | 4.3% |
| 394 | Nephroblastoma | 4.2% |
| 395 | Skin Abnormalities | 4.2% |
| 396 | Congenital Microtia | 4.2% |
| 397 | Congenital diaphragmatic hernia | 4.2% |
| 398 | Umbilical hernia | 4.2% |
| 399 | Tay-Sachs Disease | 4.1% |
| 400 | Lymphopenia | 4.1% |
| 401 | Job Syndrome | 4% |
| 402 | Leukemia, Myelomonocytic, Chronic | 4% |
| 403 | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative | 4% |
| 404 | Anemia, Pernicious | 4% |
| 405 | Familial Periodic Paralysis | 4% |
| 406 | Aphonia | 4% |
| 407 | Retropharyngeal Abscess | 4% |
| 408 | Dysphonia | 4% |
| 409 | Lactose Intolerance | 4% |
| 410 | Variegate Porphyria | 4% |
| 411 | Acute intermittent porphyria | 4% |
| 412 | Porphyria Cutanea Tarda | 4% |
| 413 | Hyperhomocysteinemia | 3.9% |
| 414 | Renal Aminoacidurias | 3.9% |
| 415 | Fanconi Syndrome | 3.9% |
| 416 | Pseudohypoaldosteronism | 3.9% |
| 417 | Liddle Syndrome | 3.9% |
| 418 | Adenomatous Polyposis Coli | 3.9% |
| 419 | Hyperlipoproteinemia Type IV | 3.9% |
| 420 | Hyperlipoproteinemia Type V | 3.9% |
| 421 | Lymphocele | 3.9% |
| 422 | Lymphoproliferative Disorders | 3.9% |
| 423 | Thymus Neoplasms | 3.9% |
| 424 | Urogenital Abnormalities | 3.8% |
| 425 | Neonatal Abstinence Syndrome | 3.8% |
| 426 | Turner Syndrome | 3.8% |
| 427 | Klinefelter Syndrome | 3.8% |
| 428 | Fetal Growth Retardation | 3.7% |
| 429 | Fetal Hypoxia | 3.7% |
| 430 | Congenital nystagmus | 3.7% |
| 431 | Fetal Alcohol Spectrum Disorders | 3.7% |
| 432 | Glycogen Storage Disease Type I | 3.7% |
| 433 | Glycogen Storage Disease Type V | 3.7% |
| 434 | Toxoplasmosis, Congenital | 3.7% |
| 435 | Anencephaly | 3.7% |
| 436 | Syphilis, Congenital | 3.7% |
| 437 | Gout | 3.6% |
| 438 | Nasopharyngitis | 3.6% |
| 439 | Eosinophilia-Myalgia Syndrome | 3.6% |
| 440 | Multiple Endocrine Neoplasia Type 1 | 3.6% |
| 441 | Pseudohypoparathyroidism | 3.6% |
| 442 | Shwartzman Phenomenon | 3.6% |
| 443 | Friedreich Ataxia | 3.6% |
| 444 | Hemangioma, Cavernous | 3.6% |
| 445 | Renal tubular acidosis | 3.6% |
| 446 | Scurvy | 3.6% |
| 447 | Purpura Fulminans | 3.6% |
| 448 | Mucocutaneous Lymph Node Syndrome | 3.4% |
| 449 | Congenital Hyperinsulinism | 3.3% |
| 450 | Chorioamnionitis | 3.3% |
| 451 | Maxillofacial Abnormalities | 3.3% |
| 452 | Dural Arteriovenous Fistula | 3.3% |
| 453 | Dextrocardia | 3.3% |
| 454 | Peritonsillar Abscess | 3.3% |
| 455 | Hypoalphalipoproteinemias | 3.3% |
| 456 | Familial Hypophosphatemic Rickets | 3.2% |
| 457 | Neutropenia | 3.2% |
| 458 | Abnormalities, Radiation-Induced | 3% |
| 459 | Glycosuria, Renal | 3% |
| 460 | Hypokalemic periodic paralysis | 3% |
| 461 | Cystinuria | 2.9% |
| 462 | Prune Belly Syndrome | 2.8% |
| 463 | Twins, Conjoined | 2.8% |
| 464 | Waardenburg Syndrome | 2.8% |
| 465 | Leukemia, Myeloid, Chronic-Phase | 2.8% |
| 466 | Ophthalmia Neonatorum | 2.7% |
| 467 | Denys-Drash Syndrome | 2.7% |
| 468 | Arthritis, Gouty | 2.7% |
| 469 | MELAS Syndrome | 2.6% |
| 470 | Anophthalmos | 2.5% |
| 471 | Anus, Imperforate | 2.5% |
| 472 | Hydranencephaly | 2.5% |
| 473 | Microphthalmos | 2.5% |
| 474 | Neural Tube Defects | 2.5% |
| 475 | Paralysis, Obstetric | 2.5% |
| 476 | Retinopathy of Prematurity | 2.5% |
| 477 | Tethered Cord Syndrome | 2.5% |
| 478 | Iniencephaly | 2.5% |
| 479 | Craniorachischisis | 2.5% |
| 480 | Limb Deformities, Congenital | 2.5% |
| 481 | Exencephaly | 2.5% |
| 482 | Septo-Optic Dysplasia | 2.5% |
| 483 | Craniofacial Abnormalities | 2.5% |
| 484 | Cortical Dysplasia | 2.5% |
| 485 | Malformations of Cortical Development | 2.5% |
| 486 | Anorectal Malformations | 2.5% |
| 487 | Bloom Syndrome | 2.5% |
| 488 | Elephantiasis | 2.5% |
| 489 | Hypersplenism | 2.5% |
| 490 | Sarcoidosis | 2.5% |
| 491 | Elephantiasis Nostras Verrucosa | 2.5% |
| 492 | Febrile Neutropenia | 2.5% |
| 493 | Acrocephalosyndactylia | 2.4% |
| 494 | Craniosynostosis | 2.4% |
| 495 | Syndactyly | 2.4% |
| 496 | Brachycephaly | 2.4% |
| 497 | Microcephaly | 2.3% |
| 498 | Macrocephaly | 2.3% |
| 499 | Blepharophimosis | 2.2% |
| 500 | Mouth Abnormalities | 2.2% |
| 501 | Esophageal Atresia | 2.2% |
| 502 | Intestinal Atresia | 2.2% |
| 503 | Horseshoe Kidney | 2.2% |
| 504 | Pectus excavatum | 2.2% |
| 505 | Klippel-Feil Syndrome | 2.2% |
| 506 | Gastroschisis | 2.2% |
| 507 | Synostosis | 2.2% |
| 508 | Noonan Syndrome | 2.2% |
| 509 | Acrodermatitis | 2.2% |
| 510 | Gianotti-Crosti Syndrome | 2.2% |
| 511 | Granuloma | 2.2% |
| 512 | Histiocytic Disorders, Malignant | 2.2% |
| 513 | Splenic Infarction | 2.2% |
| 514 | Splenic Neoplasms | 2.2% |
| 515 | Tumor Lysis Syndrome | 2.2% |
| 516 | Cleft Palate | 2.1% |
| 517 | Arthrogryposis | 2% |
| 518 | Choledochal Cyst | 2% |
| 519 | Hermaphroditism | 2% |
| 520 | Disorders of Sex Development | 2% |
| 521 | Cryptorchidism | 2% |
| 522 | Hypospadias | 2% |
| 523 | Sezary Syndrome | 2% |
| 524 | Central Nervous System Cysts | 2% |
| 525 | Dandy-Walker Syndrome | 2% |
| 526 | Leukomalacia, Periventricular | 2% |
| 527 | Nesidioblastosis | 2% |
| 528 | Splenic Rupture | 2% |
| 529 | Porencephaly | 2% |
| 530 | Lymphoma | 2% |
| 531 | Jaw Abnormalities | 1.9% |
| 532 | Thymoma | 1.9% |
| 533 | Pectus carinatum | 1.8% |
| 534 | Bladder Exstrophy | 1.8% |
| 535 | Epispadias | 1.8% |
| 536 | Multicystic Dysplastic Kidney | 1.8% |
| 537 | Poland Syndrome | 1.8% |
| 538 | Amelia | 1.7% |
| 539 | Arachnodactyly | 1.7% |
| 540 | Ectopia Cordis | 1.7% |
| 541 | Ectromelia | 1.7% |
| 542 | Hemimelia | 1.7% |
| 543 | Meningomyelocele | 1.7% |
| 544 | Phocomelia | 1.7% |
| 545 | Sirenomelia | 1.7% |
| 546 | Spina Bifida | 1.7% |
| 547 | Polydactyly | 1.7% |
| 548 | Brachydactyly | 1.7% |
| 549 | Plagiocephaly | 1.7% |
| 550 | Lower Extremity Deformities, Congenital | 1.7% |
| 551 | Upper Extremity Deformities, Congenital | 1.7% |
| 552 | Single umbilical artery | 1.7% |
| 553 | Lymphohistiocytosis, Hemophagocytic | 1.5% |
| 554 | Erdheim-Chester Disease | 1.5% |
| 555 | Micrognathism | 1.5% |
| 556 | Pierre Robin Syndrome | 1.5% |
| 557 | Aortic coarctation | 1.5% |
| 558 | Cor Triatriatum | 1.5% |
| 559 | Coronary Vessel Anomalies | 1.5% |
| 560 | Dental Enamel Hypoplasia | 1.5% |
| 561 | Patent ductus arteriosus | 1.5% |
| 562 | Ebstein Anomaly | 1.5% |
| 563 | Heart Septal Defects | 1.5% |
| 564 | Hypodontia | 1.5% |
| 565 | Macrostomia | 1.5% |
| 566 | Meningocele | 1.5% |
| 567 | Microstomia | 1.5% |
| 568 | Tetralogy of Fallot | 1.5% |
| 569 | Transposition of Great Vessels | 1.5% |
| 570 | Hypoplastic Left Heart Syndrome | 1.5% |
| 571 | May-Thurner Syndrome | 1.5% |
| 572 | Encephalocele | 1.5% |
| 573 | Craniofacial Dysostosis | 1.5% |
| 574 | Wolff-Parkinson-White Syndrome | 1.5% |
| 575 | Hyperandrogenism | 1.4% |
| 576 | Retrognathia | 1.4% |
| 577 | Malignant histiocytosis | 1.3% |
| 578 | Histiocytic sarcoma | 1.3% |
| 579 | Long QT Syndrome | 1.3% |
| 580 | Platybasia | 1.3% |
| 581 | Tricuspid Atresia | 1.3% |
| 582 | Arrhythmogenic Right Ventricular Dysplasia | 1.3% |
| 583 | Gonadal Dysgenesis | 1.3% |
| 584 | Adrenogenital Syndrome | 1.3% |
| 585 | Ovotesticular Disorders of Sex Development | 1.3% |
| 586 | Prognathism | 1.3% |
| 587 | Dermal Sinus | 1.2% |
| 588 | Spina Bifida Cystica | 1.2% |
| 589 | Spina Bifida Occulta | 1.2% |
| 590 | Lissencephaly | 1.2% |
| 591 | Polymicrogyria | 1.2% |
| 592 | Pachygyria | 1.2% |
| 593 | Schizencephaly | 1.2% |
| 594 | Periventricular Nodular Heterotopia | 1.2% |
| 595 | Splenosis | 1.2% |
| 596 | Hodgkin Disease | 1.2% |
| 597 | Lymphoma, Non-Hodgkin | 1.2% |
| 598 | Leukemia, T-Cell | 1.2% |
| 599 | Leukemia, B-Cell | 1.2% |
| 600 | Aortopulmonary Septal Defect | 1.1% |
| 601 | Double Outlet Right Ventricle | 1.1% |
| 602 | Endocardial Cushion Defects | 1.1% |
| 603 | Myocardial bridging | 1.1% |
| 604 | Aorticopulmonary Septal Defect | 1.1% |
| 605 | Composite Lymphoma | 1.1% |
| 606 | Lymphangioleiomyomatosis | 1.1% |
| 607 | Mandibulofacial Dysostosis | 1% |
| 608 | Romano-Ward Syndrome | 1% |
| 609 | Truncus Arteriosus, Persistent | 0.9% |
| 610 | Goldenhar Syndrome | 0.9% |
| 611 | Talipes | 0.8% |
| 612 | Arteriovenous fistula | 0.8% |
| 613 | Lymphoma, Follicular | 0.8% |
| 614 | T-Cell Lymphoma | 0.8% |
| 615 | Mantle cell lymphoma | 0.8% |
| 616 | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma | 0.8% |
| 617 | Leukemia, Large Granular Lymphocytic | 0.8% |
| 618 | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma | 0.8% |
| 619 | Congenital clubfoot | 0.7% |
| 620 | Vertical Talus | 0.7% |
| 621 | Lymphoma, T-Cell, Cutaneous | 0.6% |
| 622 | Lymphoma, AIDS-Related | 0.6% |
| 623 | Enteropathy-Associated T-Cell Lymphoma | 0.6% |
| 624 | Primary Effusion Lymphoma | 0.6% |
| 625 | Lymphomatoid Granulomatosis | 0.6% |
| 626 | Mycosis Fungoides | 0.5% |
| 627 | Lymphomatoid Papulosis | 0.5% |
| 628 | Plasmablastic lymphoma | 0.5% |
| 629 | Burkitt Lymphoma | 0.5% |