| 1 | Esophageal Atresia | 43.2% |
| 2 | Anus, Imperforate | 39.7% |
| 3 | Anorectal Malformations | 39.7% |
| 4 | Zollinger-Ellison syndrome | 38.6% |
| 5 | Proctocolitis | 38.4% |
| 6 | Duodenitis | 36.5% |
| 7 | Ileitis | 36.5% |
| 8 | Erosive Duodenitis | 36.5% |
| 9 | Colorectal Neoplasms | 36.4% |
| 10 | Dysentery | 35.1% |
| 11 | Enteritis | 35.1% |
| 12 | Enterocolitis | 35.1% |
| 13 | Inflammatory Bowel Diseases | 35.1% |
| 14 | Duodenal Obstruction | 34.7% |
| 15 | Choledochal Cyst | 33.3% |
| 16 | Pouchitis | 30.7% |
| 17 | Cecal Neoplasms | 30.4% |
| 18 | Duodenal Neoplasms | 30.4% |
| 19 | Intestinal Neoplasms | 29.7% |
| 20 | Colitis | 29.5% |
| 21 | Duodenogastric Reflux | 29.5% |
| 22 | Peptic Ulcer | 29.5% |
| 23 | Proctitis | 29.5% |
| 24 | Rectal Fistula | 29.3% |
| 25 | Anal Fistula | 29.3% |
| 26 | Cecal Diseases | 28.8% |
| 27 | Colonic Diseases | 28.8% |
| 28 | Ileal Diseases | 28.8% |
| 29 | Intestinal Obstruction | 28.8% |
| 30 | Intestinal Perforation | 28.8% |
| 31 | Jejunal Diseases | 28.8% |
| 32 | Pneumatosis Cystoides Intestinalis | 28.8% |
| 33 | Rectal Diseases | 28.8% |
| 34 | Cronkhite-Canada Syndrome | 28.8% |
| 35 | Intestinal Polyposis | 28.8% |
| 36 | Anus Neoplasms | 28.6% |
| 37 | Sigmoid Neoplasms | 28.6% |
| 38 | Colonic Pseudo-Obstruction | 27.8% |
| 39 | Mesenteric vascular insufficiency | 27.6% |
| 40 | Mesenteric Vascular Occlusion | 27.3% |
| 41 | Intestinal Fistula | 27.1% |
| 42 | Enterocutaneous Fistula | 27.1% |
| 43 | Crohn Disease | 26.7% |
| 44 | Enterocolitis, Neutropenic | 26.7% |
| 45 | Necrotizing Enterocolitis | 26.7% |
| 46 | Appendiceal Neoplasms | 25.6% |
| 47 | Colonic Neoplasms | 25.6% |
| 48 | Rectal Neoplasms | 25.6% |
| 49 | Adenomatous Polyposis Coli | 25.4% |
| 50 | Appendicitis | 24.6% |
| 51 | Esophagitis | 24.3% |
| 52 | Gastritis | 24.3% |
| 53 | Intestinal Diseases, Parasitic | 23.9% |
| 54 | Duodenal Ulcer | 23.9% |
| 55 | Peptic Ulcer Perforation | 23.9% |
| 56 | Gastric ulcer | 23.9% |
| 57 | Gastrointestinal Neoplasms | 23% |
| 58 | Esophageal Diseases | 22.4% |
| 59 | Gastroenteritis | 22.4% |
| 60 | Stomach Diseases | 22.4% |
| 61 | Enterocolitis, Pseudomembranous | 22.1% |
| 62 | pseudomembranous colitis | 22.1% |
| 63 | Dysentery, Bacillary | 22.1% |
| 64 | Stomach Neoplasms | 22% |
| 65 | Colonic Diseases, Functional | 21.8% |
| 66 | Fecal Incontinence | 21.8% |
| 67 | Fecal Impaction | 21.8% |
| 68 | Intussusception | 21.8% |
| 69 | Megacolon | 21.8% |
| 70 | Ileus | 21.8% |
| 71 | Meconium ileus | 21.8% |
| 72 | Colitis, Ischemic | 20.2% |
| 73 | Biliary Tract Diseases | 19.6% |
| 74 | Liver diseases | 19.6% |
| 75 | Pancreatic Diseases | 19.6% |
| 76 | Esophageal Neoplasms | 19.2% |
| 77 | Esophageal and Gastric Varices | 18.9% |
| 78 | Anal Fissure | 18.4% |
| 79 | Intestinal Pseudo-Obstruction | 18.4% |
| 80 | Irritable Bowel Syndrome | 18.4% |
| 81 | Superior Mesenteric Artery Syndrome | 18.4% |
| 82 | Neurogenic Bowel | 18.4% |
| 83 | Anal Ulcer | 18.4% |
| 84 | Gastrointestinal Hemorrhage | 17.8% |
| 85 | Hemorrhoids | 17.7% |
| 86 | Tuberculosis, Gastrointestinal | 17.6% |
| 87 | Afferent Loop Syndrome | 17.4% |
| 88 | Celiac Disease | 17.4% |
| 89 | Short Bowel Syndrome | 17.4% |
| 90 | Sprue, Tropical | 17.4% |
| 91 | Steatorrhea | 17.4% |
| 92 | Rectocele | 17.4% |
| 93 | Sprue | 17.4% |
| 94 | Rectal Prolapse | 17.3% |
| 95 | Liver neoplasms | 16.1% |
| 96 | Pancreatic Fistula | 16% |
| 97 | Beckwith-Wiedemann Syndrome | 15.7% |
| 98 | Wolf-Hirschhorn Syndrome | 15.7% |
| 99 | Digestive System Neoplasms | 15.7% |
| 100 | Gastrointestinal Stromal Tumors | 15.6% |
| 101 | Abnormalities, Drug-Induced | 15.5% |
| 102 | Situs Inversus | 15.5% |
| 103 | Holoprosencephaly | 15.3% |
| 104 | Esophageal Stenosis | 15.3% |
| 105 | Gastric Dilatation | 15.3% |
| 106 | Gastric outlet obstruction | 15.3% |
| 107 | Biliary cirrhosis | 15% |
| 108 | Giardiasis | 14.9% |
| 109 | Pruritus Ani | 14.7% |
| 110 | Peutz-Jeghers Syndrome | 14.4% |
| 111 | Bile Duct Neoplasms | 14.4% |
| 112 | gallbladder neoplasm | 14.4% |
| 113 | Lactose Intolerance | 13.7% |
| 114 | Peritoneal Neoplasms | 13.7% |
| 115 | Smith-Magenis syndrome | 13.6% |
| 116 | Cholecystolithiasis | 13.5% |
| 117 | Cri-du-Chat Syndrome | 13.4% |
| 118 | Down Syndrome | 13.4% |
| 119 | Trisomy 21 | 13.4% |
| 120 | Aicardi's syndrome | 13.2% |
| 121 | Cystic Fibrosis | 13% |
| 122 | Eye Abnormalities | 12.9% |
| 123 | Cardiovascular Abnormalities | 12.9% |
| 124 | Esophageal Perforation | 12.7% |
| 125 | Skin Abnormalities | 12.5% |
| 126 | Lymphatic Abnormalities | 12.5% |
| 127 | Congenital Microtia | 12.5% |
| 128 | Barrett Esophagus | 12.3% |
| 129 | Deglutition Disorders | 12.3% |
| 130 | Rubinstein-Taybi Syndrome | 12.3% |
| 131 | Congenital diaphragmatic hernia | 12.2% |
| 132 | Achlorhydria | 12.2% |
| 133 | Gastric Antral Vascular Ectasia | 12.2% |
| 134 | Peptic Ulcer Hemorrhage | 12.1% |
| 135 | Gastroparesis | 12.1% |
| 136 | Choledocholithiasis | 12.1% |
| 137 | Bile Duct Diseases | 12.1% |
| 138 | Cholelithiasis | 12.1% |
| 139 | Chylous Ascites | 12.1% |
| 140 | Fatty Liver | 12.1% |
| 141 | Hepatitis | 12.1% |
| 142 | Portal Hypertension | 12.1% |
| 143 | Liver Cirrhosis | 12.1% |
| 144 | Pancreatic Insufficiency | 12.1% |
| 145 | Pancreatic Neoplasm | 12.1% |
| 146 | Pancreatitis | 12.1% |
| 147 | Pneumoperitoneum | 12.1% |
| 148 | Focal Nodular Hyperplasia | 12.1% |
| 149 | Hepatic Insufficiency | 12.1% |
| 150 | Steatohepatitis | 12.1% |
| 151 | Ectodermal Dysplasia | 11.8% |
| 152 | Esophageal motility disorders | 11.8% |
| 153 | Mallory-Weiss Syndrome | 11.8% |
| 154 | Pyloric Stenosis | 11.8% |
| 155 | Aplasia Cutis Congenita | 11.8% |
| 156 | Anencephaly | 11.7% |
| 157 | Prader-Willi Syndrome | 11.7% |
| 158 | Fatty Liver, Alcoholic | 11.1% |
| 159 | Hepatitis, Alcoholic | 11.1% |
| 160 | Liver Cirrhosis, Alcoholic | 11.1% |
| 161 | Gastrointestinal Diseases | 10.7% |
| 162 | Urogenital Abnormalities | 10.7% |
| 163 | CHARGE Syndrome | 10.2% |
| 164 | Melena | 10.2% |
| 165 | Prune Belly Syndrome | 10.2% |
| 166 | Twins, Conjoined | 10.2% |
| 167 | Waardenburg Syndrome | 10.2% |
| 168 | Maxillofacial Abnormalities | 10.1% |
| 169 | Dural Arteriovenous Fistula | 10.1% |
| 170 | Kartagener Syndrome | 10.1% |
| 171 | Dextrocardia | 10% |
| 172 | Esophageal Achalasia | 10% |
| 173 | Hematemesis | 10% |
| 174 | Liver Diseases, Parasitic | 10% |
| 175 | Cryptosporidiosis | 9.7% |
| 176 | Hepatic Veno-Occlusive Disease | 9.7% |
| 177 | Pancreatic Cyst | 9.7% |
| 178 | Peliosis Hepatis | 9.7% |
| 179 | Hepatopulmonary Syndrome | 9.7% |
| 180 | Congenital Hyperinsulinism | 9.7% |
| 181 | Hemoperitoneum | 9.6% |
| 182 | Hepatomegaly | 9.6% |
| 183 | Mesenteric Panniculitis | 9.6% |
| 184 | Panniculitis, Peritoneal | 9.6% |
| 185 | Peritonitis | 9.6% |
| 186 | Peritoneal Fibrosis | 9.6% |
| 187 | Encapsulating Peritoneal Sclerosis | 9.6% |
| 188 | Biliary Fistula | 9.5% |
| 189 | Gastric Fistula | 9.5% |
| 190 | Hepatocellular Adenoma | 9.5% |
| 191 | Hepatic Vein Thrombosis | 9.5% |
| 192 | Liver Abscess | 9.5% |
| 193 | Budd-Chiari Syndrome | 9.5% |
| 194 | Diverticulitis | 9.3% |
| 195 | Dumping Syndrome | 9.3% |
| 196 | Marfan Syndrome | 9.2% |
| 197 | Genetic Diseases, Inborn | 8.9% |
| 198 | Nail-Patella Syndrome | 8.8% |
| 199 | Xeroderma | 8.7% |
| 200 | Porphyrias, Hepatic | 8.7% |
| 201 | Mobius Syndrome | 8.7% |
| 202 | Cholangitis | 8.5% |
| 203 | Cholecystitis | 8.5% |
| 204 | Cholestasis | 8.5% |
| 205 | Common Bile Duct Diseases | 8.5% |
| 206 | Hepatitis, Chronic | 8.5% |
| 207 | Liver Failure | 8.5% |
| 208 | Pancreatitis, Chronic | 8.5% |
| 209 | Non-alcoholic Fatty Liver Disease | 8.5% |
| 210 | Chronic active hepatitis | 8.5% |
| 211 | Liver Abscess, Amebic | 8.4% |
| 212 | Liver Neoplasms, Experimental | 8.4% |
| 213 | Anophthalmos | 8.2% |
| 214 | Hydranencephaly | 8.2% |
| 215 | Microphthalmos | 8.2% |
| 216 | Neural Tube Defects | 8.2% |
| 217 | Tethered Cord Syndrome | 8.2% |
| 218 | Iniencephaly | 8.2% |
| 219 | Craniorachischisis | 8.2% |
| 220 | Limb Deformities, Congenital | 8.2% |
| 221 | Exencephaly | 8.2% |
| 222 | Septo-Optic Dysplasia | 8.2% |
| 223 | Craniofacial Abnormalities | 8.2% |
| 224 | Cortical Dysplasia | 8.2% |
| 225 | Malformations of Cortical Development | 8.2% |
| 226 | Chemical and Drug Induced Liver Injury | 8.1% |
| 227 | Zellweger Syndrome | 8.1% |
| 228 | Bloom Syndrome | 8.1% |
| 229 | Scimitar Syndrome | 8% |
| 230 | Hepatorenal Syndrome | 7.9% |
| 231 | Diverticulum | 7.9% |
| 232 | Diverticulosis | 7.9% |
| 233 | Microcephaly | 7.8% |
| 234 | Macrocephaly | 7.8% |
| 235 | Alstrom Syndrome | 7.7% |
| 236 | Polycystic Kidney Diseases | 7.6% |
| 237 | Williams Syndrome | 7.6% |
| 238 | Abnormalities, Radiation-Induced | 7.6% |
| 239 | Acrocephalosyndactylia | 7.5% |
| 240 | Craniosynostosis | 7.5% |
| 241 | Syndactyly | 7.5% |
| 242 | Brachycephaly | 7.5% |
| 243 | Laryngopharyngeal Reflux | 7.4% |
| 244 | Cockayne Syndrome | 7.4% |
| 245 | Fragile X Syndrome | 7.4% |
| 246 | Fetal Diseases | 7.1% |
| 247 | Hepatitis B, Chronic | 7.1% |
| 248 | Hepatitis C, Chronic | 7.1% |
| 249 | Classical Lissencephalies and Subcortical Band Heterotopias | 7% |
| 250 | Hepatitis, Animal | 7% |
| 251 | Hepatitis, Viral, Human | 7% |
| 252 | Porencephaly | 7% |
| 253 | Turner Syndrome | 6.9% |
| 254 | Blepharophimosis | 6.9% |
| 255 | Intestinal Diseases | 6.9% |
| 256 | Laryngostenosis | 6.9% |
| 257 | Mouth Abnormalities | 6.9% |
| 258 | Retinal Dysplasia | 6.9% |
| 259 | Aniridia | 6.8% |
| 260 | Intestinal Atresia | 6.8% |
| 261 | Horseshoe Kidney | 6.8% |
| 262 | Pectus excavatum | 6.8% |
| 263 | Klippel-Feil Syndrome | 6.8% |
| 264 | Gastroschisis | 6.8% |
| 265 | Synostosis | 6.8% |
| 266 | Liver Cirrhosis, Experimental | 6.8% |
| 267 | Pancreatic Pseudocyst | 6.8% |
| 268 | Acrodermatitis | 6.7% |
| 269 | Lymphangiectasis, Intestinal | 6.7% |
| 270 | Gianotti-Crosti Syndrome | 6.7% |
| 271 | Cholestasis, Extrahepatic | 6.7% |
| 272 | Biliary Dyskinesia | 6.7% |
| 273 | Cholangitis, Sclerosing | 6.7% |
| 274 | Epidermolysis Bullosa | 6.7% |
| 275 | Liver Failure, Acute | 6.7% |
| 276 | Acalculous Cholecystitis | 6.7% |
| 277 | End Stage Liver Disease | 6.7% |
| 278 | Noonan Syndrome | 6.7% |
| 279 | Pancreatitis, Alcoholic | 6.7% |
| 280 | Nesidioblastosis | 6.6% |
| 281 | Ichthyosis, X-Linked | 6.6% |
| 282 | Primary Ciliary Dyskinesia | 6.6% |
| 283 | Carcinoma, Pancreatic Ductal | 6.6% |
| 284 | Smith-Lemli-Opitz Syndrome | 6.6% |
| 285 | Cleft Palate | 6.4% |
| 286 | Jaw Abnormalities | 6.2% |
| 287 | Variegate Porphyria | 6.2% |
| 288 | Acute intermittent porphyria | 6.2% |
| 289 | Porphyria Cutanea Tarda | 6.2% |
| 290 | Poland Syndrome | 6.1% |
| 291 | Amelia | 6% |
| 292 | Arachnodactyly | 6% |
| 293 | Ectopia Cordis | 6% |
| 294 | Ectromelia | 6% |
| 295 | Hemimelia | 6% |
| 296 | Meningomyelocele | 6% |
| 297 | Phocomelia | 6% |
| 298 | Sirenomelia | 6% |
| 299 | Spina Bifida | 6% |
| 300 | Polydactyly | 6% |
| 301 | Brachydactyly | 6% |
| 302 | Plagiocephaly | 6% |
| 303 | Lower Extremity Deformities, Congenital | 6% |
| 304 | Upper Extremity Deformities, Congenital | 6% |
| 305 | Single umbilical artery | 6% |
| 306 | Arthrogryposis | 5.9% |
| 307 | Choanal Atresia | 5.9% |
| 308 | Tracheobronchomegaly | 5.9% |
| 309 | Laryngocele | 5.9% |
| 310 | Hermaphroditism | 5.9% |
| 311 | Disorders of Sex Development | 5.9% |
| 312 | Massive Hepatic Necrosis | 5.9% |
| 313 | Emphysematous Cholecystitis | 5.9% |
| 314 | Sphincter of Oddi Dysfunction | 5.9% |
| 315 | Cryptorchidism | 5.8% |
| 316 | Hypospadias | 5.8% |
| 317 | insulinoma | 5.8% |
| 318 | Gastrinoma | 5.8% |
| 319 | Glucagonoma | 5.8% |
| 320 | Central Nervous System Cysts | 5.8% |
| 321 | Dandy-Walker Syndrome | 5.8% |
| 322 | Klinefelter Syndrome | 5.7% |
| 323 | POEMS Syndrome | 5.7% |
| 324 | Fascioliasis | 5.7% |
| 325 | Hepatolenticular Degeneration | 5.7% |
| 326 | Echinococcosis, Hepatic | 5.6% |
| 327 | Polycystic Kidney, Autosomal Dominant | 5.6% |
| 328 | Chemical and Drug Induced Liver Injury, Chronic | 5.6% |
| 329 | Reye Syndrome | 5.6% |
| 330 | Autoimmune hepatitis | 5.4% |
| 331 | Pseudoxanthoma Elasticum | 5.4% |
| 332 | Sjogren-Larsson Syndrome | 5.3% |
| 333 | Micrognathism | 5.2% |
| 334 | Pierre Robin Syndrome | 5.2% |
| 335 | Vipoma | 5.2% |
| 336 | Abdominal Cramps | 5.2% |
| 337 | Amniotic Band Syndrome | 5.2% |
| 338 | Asphyxia Neonatorum | 5.2% |
| 339 | Infant, Premature, Diseases | 5.2% |
| 340 | Meconium Aspiration Syndrome | 5.2% |
| 341 | Laryngomalacia | 5.2% |
| 342 | Infantile Colic | 5.2% |
| 343 | Pectus carinatum | 5.1% |
| 344 | Bladder Exstrophy | 5.1% |
| 345 | Epispadias | 5.1% |
| 346 | Multicystic Dysplastic Kidney | 5% |
| 347 | Aortic coarctation | 5% |
| 348 | Cor Triatriatum | 5% |
| 349 | Coronary Vessel Anomalies | 5% |
| 350 | Dental Enamel Hypoplasia | 5% |
| 351 | Patent ductus arteriosus | 5% |
| 352 | Ebstein Anomaly | 5% |
| 353 | Heart Septal Defects | 5% |
| 354 | Hypodontia | 5% |
| 355 | Macrostomia | 5% |
| 356 | Meningocele | 5% |
| 357 | Microstomia | 5% |
| 358 | Tetralogy of Fallot | 5% |
| 359 | Transposition of Great Vessels | 5% |
| 360 | Hypoplastic Left Heart Syndrome | 5% |
| 361 | May-Thurner Syndrome | 5% |
| 362 | Encephalocele | 5% |
| 363 | Craniofacial Dysostosis | 5% |
| 364 | Dermal Sinus | 5% |
| 365 | Spina Bifida Cystica | 5% |
| 366 | Spina Bifida Occulta | 5% |
| 367 | Lissencephaly | 5% |
| 368 | Polymicrogyria | 5% |
| 369 | Pachygyria | 5% |
| 370 | Schizencephaly | 5% |
| 371 | Periventricular Nodular Heterotopia | 5% |
| 372 | Kallmann Syndrome | 5% |
| 373 | Wolff-Parkinson-White Syndrome | 5% |
| 374 | Charcot-Marie-Tooth Disease | 4.9% |
| 375 | Antley-Bixler Syndrome Phenotype | 4.9% |
| 376 | Xeroderma Pigmentosum | 4.9% |
| 377 | Hyperkeratosis, Epidermolytic | 4.9% |
| 378 | Retrognathia | 4.7% |
| 379 | Hepatitis, Viral, Animal | 4.7% |
| 380 | Hepatitis E | 4.6% |
| 381 | Hepatitis B | 4.5% |
| 382 | Hepatitis C | 4.5% |
| 383 | Hepatitis A | 4.5% |
| 384 | Hepatic Encephalopathy | 4.4% |
| 385 | Hyperandrogenism | 4.4% |
| 386 | Basal Cell Nevus Syndrome | 4.4% |
| 387 | Tuberous Sclerosis | 4.4% |
| 388 | CREST Syndrome | 4.4% |
| 389 | Long QT Syndrome | 4.3% |
| 390 | Platybasia | 4.3% |
| 391 | Tricuspid Atresia | 4.3% |
| 392 | Arrhythmogenic Right Ventricular Dysplasia | 4.3% |
| 393 | Gonadal Dysgenesis | 4.3% |
| 394 | Neoplastic Syndromes, Hereditary | 4.3% |
| 395 | Bronchomalacia | 4.3% |
| 396 | Adrenogenital Syndrome | 4.3% |
| 397 | Tracheomalacia | 4.3% |
| 398 | Ovotesticular Disorders of Sex Development | 4.3% |
| 399 | Prognathism | 4.3% |
| 400 | Refsum Disease | 4.2% |
| 401 | Aortopulmonary Septal Defect | 4.1% |
| 402 | Double Outlet Right Ventricle | 4.1% |
| 403 | Endocardial Cushion Defects | 4.1% |
| 404 | Myocardial bridging | 4.1% |
| 405 | Aorticopulmonary Septal Defect | 4.1% |
| 406 | Anemia, Neonatal | 4.1% |
| 407 | Multiple Epiphyseal Dysplasia | 4.1% |
| 408 | Osteochondrodysplasias | 4.1% |
| 409 | Pelger-Huet Anomaly | 4.1% |
| 410 | Persistent Fetal Circulation Syndrome | 4.1% |
| 411 | Werner Syndrome | 4.1% |
| 412 | Myasthenic Syndromes, Congenital | 4.1% |
| 413 | Umbilical hernia | 4.1% |
| 414 | Anemia, Sickle Cell | 3.8% |
| 415 | Thalassemia | 3.8% |
| 416 | Muscular Dystrophy, Duchenne | 3.8% |
| 417 | Truncus Arteriosus, Persistent | 3.7% |
| 418 | Goldenhar Syndrome | 3.7% |
| 419 | Albinism | 3.7% |
| 420 | Mandibulofacial Dysostosis | 3.5% |
| 421 | Dwarfism | 3.5% |
| 422 | Romano-Ward Syndrome | 3.5% |
| 423 | Neonatal Abstinence Syndrome | 3.5% |
| 424 | Fetal Growth Retardation | 3.4% |
| 425 | Muscular Dystrophy | 3.4% |
| 426 | Osteogenesis Imperfecta | 3.4% |
| 427 | Familial Mediterranean Fever | 3.4% |
| 428 | Fetal Hypoxia | 3.4% |
| 429 | Congenital nystagmus | 3.4% |
| 430 | Fetal Alcohol Spectrum Disorders | 3.4% |
| 431 | Toxoplasmosis, Congenital | 3.4% |
| 432 | Syphilis, Congenital | 3.4% |
| 433 | Rett Syndrome | 3.3% |
| 434 | Mucopolysaccharidosis II | 3.2% |
| 435 | Talipes | 3.2% |
| 436 | Menkes Kinky Hair Syndrome | 3% |
| 437 | Congenital clubfoot | 3% |
| 438 | Vertical Talus | 3% |
| 439 | Wiskott-Aldrich Syndrome | 3% |
| 440 | Autoimmune Lymphoproliferative Syndrome | 2.9% |
| 441 | Chorioamnionitis | 2.9% |
| 442 | Angioedemas, Hereditary | 2.9% |
| 443 | Sickle Cell Trait | 2.8% |
| 444 | Arteriovenous fistula | 2.8% |
| 445 | Paralysis, Obstetric | 2.7% |
| 446 | Retinopathy of Prematurity | 2.7% |
| 447 | Amino Acid Metabolism, Inborn Errors | 2.7% |
| 448 | Carbohydrate Metabolism, Inborn Errors | 2.7% |
| 449 | Metal Metabolism, Inborn Errors | 2.7% |
| 450 | Progeria | 2.7% |
| 451 | Lysosomal Storage Diseases | 2.7% |
| 452 | Cytochrome-c Oxidase Deficiency | 2.7% |
| 453 | Peroxisomal Disorders | 2.7% |
| 454 | Neuronal Ceroid-Lipofuscinoses | 2.7% |
| 455 | Bronchopulmonary Dysplasia | 2.7% |
| 456 | Myotonic Dystrophy | 2.7% |
| 457 | Rift Valley Fever | 2.6% |
| 458 | Adrenoleukodystrophy | 2.5% |
| 459 | Fabry Disease | 2.3% |
| 460 | Amyloid Neuropathies, Familial | 2.3% |
| 461 | Respiratory Distress Syndrome, Newborn | 2.3% |
| 462 | Cutis Laxa | 2.3% |
| 463 | Denys-Drash Syndrome | 2.3% |
| 464 | Retinitis Pigmentosa | 2.3% |
| 465 | Pigmentary retinopathy | 2.3% |
| 466 | Porokeratosis | 2.2% |
| 467 | Keratoderma, Palmoplantar | 2.2% |
| 468 | Chronic granulomatous disease | 2.2% |
| 469 | Acute Chest Syndrome | 2.2% |
| 470 | Welander Distal Myopathy | 2.2% |
| 471 | Ophthalmia Neonatorum | 2.2% |
| 472 | Glycogen storage disease type II | 2.2% |
| 473 | Galactosemias | 2.2% |
| 474 | Urea Cycle Disorders, Inborn | 2.2% |
| 475 | Tyrosinemias | 2.2% |
| 476 | Hydrops Fetalis | 2.2% |
| 477 | Mucopolysaccharidosis III | 2% |
| 478 | Ataxia Telangiectasia | 2% |
| 479 | Alkaptonuria | 2% |
| 480 | Glycogen Storage Disease | 2% |
| 481 | Hypophosphatasia | 2% |
| 482 | Propionic acidemia | 2% |
| 483 | Dihydropyrimidine Dehydrogenase Deficiency | 2% |
| 484 | Cystinosis | 2% |
| 485 | Optic Atrophy, Hereditary, Leber | 2% |
| 486 | Hyperphosphaturia | 2% |
| 487 | Duane Retraction Syndrome | 2% |
| 488 | Canavan Disease | 1.9% |
| 489 | Alexander Disease | 1.9% |
| 490 | Myotonia Congenita | 1.9% |
| 491 | Thrombasthenia | 1.9% |
| 492 | Antithrombin III Deficiency | 1.9% |
| 493 | Protein C Deficiency | 1.9% |
| 494 | Brain Diseases, Metabolic, Inborn | 1.9% |
| 495 | Afibrinogenemia | 1.9% |
| 496 | Dystonia Musculorum Deformans | 1.9% |
| 497 | Factor VII Deficiency | 1.9% |
| 498 | Factor X Deficiency | 1.9% |
| 499 | Factor XII Deficiency | 1.9% |
| 500 | Hemophilia A | 1.9% |
| 501 | Leukomalacia, Periventricular | 1.9% |
| 502 | Activated Protein C Resistance | 1.9% |
| 503 | Factor II deficiency | 1.9% |
| 504 | Factor VIII Deficiency | 1.9% |
| 505 | Factor V deficiency | 1.9% |
| 506 | Factor XI Deficiency | 1.9% |
| 507 | Hypoprothrombinemias | 1.9% |
| 508 | Fanconi Anemia | 1.9% |
| 509 | Lafora Disease | 1.9% |
| 510 | Unverricht-Lundborg Syndrome | 1.9% |
| 511 | Anemia, Diamond-Blackfan | 1.9% |
| 512 | Homocystinuria | 1.8% |
| 513 | Gaucher Disease | 1.8% |
| 514 | Leigh Disease | 1.8% |
| 515 | Multiple Endocrine Neoplasia | 1.7% |
| 516 | Congenital Hypothyroidism | 1.7% |
| 517 | Dermatitis, Atopic | 1.7% |
| 518 | Hyaline Membrane Disease | 1.7% |
| 519 | Hypolipoproteinemias | 1.7% |
| 520 | Papillon-Lefevre Disease | 1.7% |
| 521 | Glycogen Storage Disease Type I | 1.7% |
| 522 | Glycogen Storage Disease Type V | 1.7% |
| 523 | Hyperlipidemia, Familial Combined | 1.7% |
| 524 | Hyperlipoproteinemia Type III | 1.7% |
| 525 | Tay-Sachs Disease | 1.6% |
| 526 | Carbamoyl-Phosphate Synthase I Deficiency Disease | 1.6% |
| 527 | Niemann-Pick Disease, Type C | 1.6% |
| 528 | Kernicterus | 1.5% |
| 529 | Behcet Syndrome | 1.5% |
| 530 | Familial Periodic Paralysis | 1.4% |
| 531 | Hyperhomocysteinemia | 1.4% |
| 532 | Renal Aminoacidurias | 1.4% |
| 533 | Fanconi Syndrome | 1.4% |
| 534 | Pseudohypoaldosteronism | 1.4% |
| 535 | Liddle Syndrome | 1.4% |
| 536 | Hyperlipoproteinemia Type IV | 1.4% |
| 537 | Hyperlipoproteinemia Type V | 1.4% |
| 538 | Hypoalphalipoproteinemias | 1.4% |
| 539 | Huntington Disease | 1.3% |
| 540 | Gout | 1.3% |
| 541 | Multiple Endocrine Neoplasia Type 1 | 1.3% |
| 542 | Pseudohypoparathyroidism | 1.3% |
| 543 | Friedreich Ataxia | 1.2% |
| 544 | Renal tubular acidosis | 1.2% |
| 545 | Nephroblastoma | 1.2% |
| 546 | Hypokalemic periodic paralysis | 1.2% |
| 547 | Cystinuria | 1.2% |
| 548 | Familial Hypophosphatemic Rickets | 1.1% |
| 549 | Arthritis, Gouty | 1% |
| 550 | Glycosuria, Renal | 1% |
| 551 | MELAS Syndrome | 0.8% |