| 1 | Abdominal Cramps | 20.9% |
| 2 | Amniotic Band Syndrome | 20.9% |
| 3 | Asphyxia Neonatorum | 20.9% |
| 4 | Infant, Premature, Diseases | 20.9% |
| 5 | Infantile Colic | 20.9% |
| 6 | Frostbite | 18.2% |
| 7 | Anemia, Neonatal | 15.5% |
| 8 | Persistent Fetal Circulation Syndrome | 15.5% |
| 9 | Umbilical hernia | 15.3% |
| 10 | Athletic Injuries | 14.6% |
| 11 | Hand Injuries | 14.6% |
| 12 | Soft Tissue Injuries | 14.6% |
| 13 | Sprain | 14.6% |
| 14 | Sprains and Strains | 14.6% |
| 15 | Tendon Injuries | 14.6% |
| 16 | Laceration | 14.6% |
| 17 | Wounds, Penetrating | 14.6% |
| 18 | Heat Cramps | 14.6% |
| 19 | Rupture | 14.6% |
| 20 | Cystic Fibrosis | 14.1% |
| 21 | Crush syndrome | 14% |
| 22 | Femoral Fractures | 14% |
| 23 | Tibial Fractures | 14% |
| 24 | Hip Fractures | 13.7% |
| 25 | Neonatal Abstinence Syndrome | 12.7% |
| 26 | Xeroderma | 12.5% |
| 27 | Mobius Syndrome | 12.5% |
| 28 | Congenital nystagmus | 12.2% |
| 29 | Deformity | 12.2% |
| 30 | Genetic Diseases, Inborn | 12.2% |
| 31 | Toxoplasmosis, Congenital | 12.1% |
| 32 | Syphilis, Congenital | 12.1% |
| 33 | Chilblains | 12.1% |
| 34 | Spinal Fractures | 12.1% |
| 35 | Meconium Aspiration Syndrome | 11.9% |
| 36 | Trauma, Nervous System | 11.3% |
| 37 | Hip Dislocation | 11.1% |
| 38 | Shoulder Dislocation | 11.1% |
| 39 | Splenic Rupture | 11.1% |
| 40 | Hip Dysplasia | 11.1% |
| 41 | Bites and Stings | 10.9% |
| 42 | Extravasation of Diagnostic and Therapeutic Materials | 10.9% |
| 43 | Vascular System Injuries | 10.9% |
| 44 | Tympanic Membrane Perforation | 10.9% |
| 45 | Tooth Injuries | 10.9% |
| 46 | Asphyxia | 10.7% |
| 47 | Esophageal Perforation | 10.7% |
| 48 | Shock, Traumatic | 10.7% |
| 49 | Self Mutilation | 10.6% |
| 50 | Retinopathy of Prematurity | 10.3% |
| 51 | Congenital Hyperinsulinism | 10.2% |
| 52 | Iliotibial Band Syndrome | 10.2% |
| 53 | Bronchopulmonary Dysplasia | 10.1% |
| 54 | Human Bite | 9.3% |
| 55 | Contusions | 9.3% |
| 56 | Decompression Sickness | 9.3% |
| 57 | Finger Injuries | 9.3% |
| 58 | Flail Chest | 9.3% |
| 59 | Fractures, Closed | 9.3% |
| 60 | Pathological fracture | 9.3% |
| 61 | Heart Injuries | 9.3% |
| 62 | Heat Exhaustion | 9.3% |
| 63 | Heat Stroke | 9.3% |
| 64 | Knee Injuries | 9.3% |
| 65 | Foot Injuries | 9.3% |
| 66 | Decapitation | 9.3% |
| 67 | Ankle Fracture | 9.3% |
| 68 | Avulsion fracture | 9.3% |
| 69 | Compression fracture | 9.3% |
| 70 | Osteoporotic Fractures | 9.3% |
| 71 | Fetal Diseases | 9.1% |
| 72 | Spinal Cord Injuries | 8.6% |
| 73 | Drowning | 8.5% |
| 74 | Eye Burns | 8.4% |
| 75 | Respiratory Distress Syndrome, Newborn | 8.3% |
| 76 | Beckwith-Wiedemann Syndrome | 8.1% |
| 77 | Wolf-Hirschhorn Syndrome | 8.1% |
| 78 | Splenosis | 8.1% |
| 79 | Ichthyosis, X-Linked | 7.8% |
| 80 | Ophthalmia Neonatorum | 7.4% |
| 81 | Aicardi's syndrome | 7.2% |
| 82 | Craniocerebral Trauma | 7% |
| 83 | Tendinitis | 7% |
| 84 | Lung Injury | 7% |
| 85 | Tendinopathy | 7% |
| 86 | Abnormalities, Drug-Induced | 7% |
| 87 | Situs Inversus | 7% |
| 88 | Foreign-Body Reaction | 6.9% |
| 89 | Insect Bites and Stings | 6.9% |
| 90 | Sunburn | 6.9% |
| 91 | Tooth Avulsion | 6.9% |
| 92 | Conus Medullaris Syndrome | 6.9% |
| 93 | Radiation injury | 6.9% |
| 94 | CHARGE Syndrome | 6.8% |
| 95 | Near Drowning | 6.8% |
| 96 | Osteoradionecrosis | 6.8% |
| 97 | Pseudarthrosis | 6.8% |
| 98 | Smoke Inhalation Injury | 6.8% |
| 99 | Smith-Magenis syndrome | 6.8% |
| 100 | Abnormalities, Radiation-Induced | 6.7% |
| 101 | Cri-du-Chat Syndrome | 6.7% |
| 102 | Down Syndrome | 6.7% |
| 103 | Trisomy 21 | 6.7% |
| 104 | Leukomalacia, Periventricular | 6.7% |
| 105 | Holoprosencephaly | 6.7% |
| 106 | Nesidioblastosis | 6.6% |
| 107 | Sjogren-Larsson Syndrome | 6.4% |
| 108 | Brain Concussion | 6.3% |
| 109 | Hyaline Membrane Disease | 6% |
| 110 | Hyperkeratosis, Epidermolytic | 5.9% |
| 111 | Ectodermal Dysplasia | 5.8% |
| 112 | Aplasia Cutis Congenita | 5.8% |
| 113 | Brain Contusion | 5.8% |
| 114 | Nail-Patella Syndrome | 5.7% |
| 115 | Prader-Willi Syndrome | 5.7% |
| 116 | Neoplasms, Radiation-Induced | 5.7% |
| 117 | Fragile X Syndrome | 5.6% |
| 118 | Peripheral Nerve Injuries | 5.6% |
| 119 | Medial Tibial Stress Syndrome | 5.6% |
| 120 | Rubinstein-Taybi Syndrome | 5.5% |
| 121 | Eye Abnormalities | 5.5% |
| 122 | Neoplastic Syndromes, Hereditary | 5.5% |
| 123 | Cardiovascular Abnormalities | 5.5% |
| 124 | Uterine Rupture | 5.4% |
| 125 | Central Cord Syndrome | 5.4% |
| 126 | Skin Abnormalities | 5.3% |
| 127 | Lymphatic Abnormalities | 5.3% |
| 128 | Congenital Microtia | 5.3% |
| 129 | Multiple Epiphyseal Dysplasia | 5.2% |
| 130 | Osteochondrodysplasias | 5.2% |
| 131 | Pelger-Huet Anomaly | 5.2% |
| 132 | Werner Syndrome | 5.2% |
| 133 | Myasthenic Syndromes, Congenital | 5.2% |
| 134 | Congenital diaphragmatic hernia | 5.1% |
| 135 | Facial Injuries | 5.1% |
| 136 | Granuloma, Foreign-Body | 5.1% |
| 137 | Enthesopathy | 5.1% |
| 138 | Kernicterus | 5.1% |
| 139 | Kartagener Syndrome | 5% |
| 140 | Cockayne Syndrome | 5% |
| 141 | Uterine Perforation | 5% |
| 142 | Marfan Syndrome | 4.9% |
| 143 | Alstrom Syndrome | 4.8% |
| 144 | Anencephaly | 4.7% |
| 145 | Cardiotoxicity | 4.6% |
| 146 | Leukemia, Radiation-Induced | 4.6% |
| 147 | Familial Mediterranean Fever | 4.5% |
| 148 | Prune Belly Syndrome | 4.5% |
| 149 | Twins, Conjoined | 4.5% |
| 150 | Waardenburg Syndrome | 4.5% |
| 151 | Radiation Pneumonitis | 4.5% |
| 152 | Radiation Fibrosis | 4.5% |
| 153 | Aortic Rupture | 4.5% |
| 154 | Anemia, Sickle Cell | 4.5% |
| 155 | Thalassemia | 4.5% |
| 156 | Muscular Dystrophy, Duchenne | 4.4% |
| 157 | Polycystic Kidney Diseases | 4.4% |
| 158 | Williams Syndrome | 4.4% |
| 159 | Urogenital Abnormalities | 4.3% |
| 160 | Dwarfism | 4.3% |
| 161 | Primary Ciliary Dyskinesia | 4.2% |
| 162 | Smith-Lemli-Opitz Syndrome | 4.1% |
| 163 | Fetal Growth Retardation | 4.1% |
| 164 | Albinism | 4.1% |
| 165 | Muscular Dystrophy | 4.1% |
| 166 | Osteogenesis Imperfecta | 4.1% |
| 167 | Fetal Hypoxia | 4.1% |
| 168 | Fetal Alcohol Spectrum Disorders | 4.1% |
| 169 | Brain Injuries | 4.1% |
| 170 | Coma, Post-Head Injury | 4% |
| 171 | Carpal Tunnel Syndrome | 4% |
| 172 | Retinal Dysplasia | 4% |
| 173 | Rett Syndrome | 4% |
| 174 | Maxillofacial Abnormalities | 4% |
| 175 | Dural Arteriovenous Fistula | 4% |
| 176 | Aniridia | 3.9% |
| 177 | Dextrocardia | 3.9% |
| 178 | Epidermolysis Bullosa | 3.8% |
| 179 | Radiation Injuries, Experimental | 3.8% |
| 180 | Brain Hemorrhage, Traumatic | 3.6% |
| 181 | Classical Lissencephalies and Subcortical Band Heterotopias | 3.6% |
| 182 | Mucopolysaccharidosis II | 3.6% |
| 183 | Kallmann Syndrome | 3.5% |
| 184 | Eye Injuries | 3.5% |
| 185 | Anophthalmos | 3.4% |
| 186 | Anus, Imperforate | 3.4% |
| 187 | Hydranencephaly | 3.4% |
| 188 | Microphthalmos | 3.4% |
| 189 | Neural Tube Defects | 3.4% |
| 190 | Tethered Cord Syndrome | 3.4% |
| 191 | Iniencephaly | 3.4% |
| 192 | Craniorachischisis | 3.4% |
| 193 | Limb Deformities, Congenital | 3.4% |
| 194 | Exencephaly | 3.4% |
| 195 | Septo-Optic Dysplasia | 3.4% |
| 196 | Craniofacial Abnormalities | 3.4% |
| 197 | Cortical Dysplasia | 3.4% |
| 198 | Autoimmune Lymphoproliferative Syndrome | 3.4% |
| 199 | Malformations of Cortical Development | 3.4% |
| 200 | Anorectal Malformations | 3.4% |
| 201 | Amino Acid Metabolism, Inborn Errors | 3.4% |
| 202 | Bloom Syndrome | 3.4% |
| 203 | Carbohydrate Metabolism, Inborn Errors | 3.4% |
| 204 | Chorioamnionitis | 3.4% |
| 205 | Metal Metabolism, Inborn Errors | 3.4% |
| 206 | Progeria | 3.4% |
| 207 | Lysosomal Storage Diseases | 3.4% |
| 208 | Cytochrome-c Oxidase Deficiency | 3.4% |
| 209 | Peroxisomal Disorders | 3.4% |
| 210 | Angioedemas, Hereditary | 3.4% |
| 211 | Wiskott-Aldrich Syndrome | 3.3% |
| 212 | Brain Injuries, Diffuse | 3.3% |
| 213 | Traumatic Brain Injury | 3.3% |
| 214 | Cubital Tunnel Syndrome | 3.3% |
| 215 | Sickle Cell Trait | 3.3% |
| 216 | Polycystic Kidney, Autosomal Dominant | 3.3% |
| 217 | Menkes Kinky Hair Syndrome | 3.3% |
| 218 | Tuberous Sclerosis | 3.3% |
| 219 | Neuronal Ceroid-Lipofuscinoses | 3.1% |
| 220 | Microcephaly | 3% |
| 221 | Macrocephaly | 3% |
| 222 | Refsum Disease | 3% |
| 223 | Scimitar Syndrome | 3% |
| 224 | Pseudoxanthoma Elasticum | 3% |
| 225 | Diffuse Axonal Injury | 3% |
| 226 | Myotonic Dystrophy | 2.9% |
| 227 | Craniosynostosis | 2.8% |
| 228 | Syndactyly | 2.8% |
| 229 | Brachycephaly | 2.8% |
| 230 | Vertebral Artery Dissection | 2.8% |
| 231 | Charcot-Marie-Tooth Disease | 2.8% |
| 232 | Antley-Bixler Syndrome Phenotype | 2.8% |
| 233 | Turner Syndrome | 2.8% |
| 234 | Pneumocephalus | 2.8% |
| 235 | Blepharophimosis | 2.8% |
| 236 | Laryngostenosis | 2.8% |
| 237 | Mouth Abnormalities | 2.8% |
| 238 | Olfactory Nerve Injuries | 2.8% |
| 239 | Cerebrospinal Fluid Otorrhea | 2.8% |
| 240 | Cerebrospinal Fluid Rhinorrhea | 2.8% |
| 241 | Zellweger Syndrome | 2.8% |
| 242 | Epilepsy, Post-Traumatic | 2.7% |
| 243 | Cutis Laxa | 2.7% |
| 244 | Esophageal Atresia | 2.7% |
| 245 | Intestinal Atresia | 2.7% |
| 246 | Horseshoe Kidney | 2.7% |
| 247 | Pectus excavatum | 2.7% |
| 248 | Porencephaly | 2.7% |
| 249 | Klippel-Feil Syndrome | 2.7% |
| 250 | Retinitis Pigmentosa | 2.7% |
| 251 | Gastroschisis | 2.7% |
| 252 | Synostosis | 2.7% |
| 253 | Pigmentary retinopathy | 2.7% |
| 254 | Klinefelter Syndrome | 2.7% |
| 255 | Acrodermatitis | 2.7% |
| 256 | Lymphangiectasis, Intestinal | 2.7% |
| 257 | Xeroderma Pigmentosum | 2.7% |
| 258 | Porokeratosis | 2.7% |
| 259 | Gianotti-Crosti Syndrome | 2.7% |
| 260 | Keratoderma, Palmoplantar | 2.7% |
| 261 | Acrocephalosyndactylia | 2.7% |
| 262 | Chronic granulomatous disease | 2.7% |
| 263 | Welander Distal Myopathy | 2.7% |
| 264 | Adrenoleukodystrophy | 2.6% |
| 265 | Amyloid Neuropathies, Familial | 2.6% |
| 266 | Corneal Scar | 2.5% |
| 267 | Hepatolenticular Degeneration | 2.5% |
| 268 | Amelia | 2.5% |
| 269 | Arachnodactyly | 2.5% |
| 270 | Ectopia Cordis | 2.5% |
| 271 | Ectromelia | 2.5% |
| 272 | Hemimelia | 2.5% |
| 273 | Meningomyelocele | 2.5% |
| 274 | Noonan Syndrome | 2.5% |
| 275 | Phocomelia | 2.5% |
| 276 | Sirenomelia | 2.5% |
| 277 | Spina Bifida | 2.5% |
| 278 | Polydactyly | 2.5% |
| 279 | Brachydactyly | 2.5% |
| 280 | Plagiocephaly | 2.5% |
| 281 | Lower Extremity Deformities, Congenital | 2.5% |
| 282 | Upper Extremity Deformities, Congenital | 2.5% |
| 283 | Single umbilical artery | 2.5% |
| 284 | Acute Chest Syndrome | 2.5% |
| 285 | Alkaptonuria | 2.5% |
| 286 | Glycogen Storage Disease | 2.5% |
| 287 | Hypophosphatasia | 2.5% |
| 288 | Propionic acidemia | 2.5% |
| 289 | Dihydropyrimidine Dehydrogenase Deficiency | 2.5% |
| 290 | Cystinosis | 2.5% |
| 291 | Carotid Artery Injuries | 2.5% |
| 292 | Fabry Disease | 2.5% |
| 293 | Galactosemias | 2.5% |
| 294 | Urea Cycle Disorders, Inborn | 2.5% |
| 295 | Tyrosinemias | 2.5% |
| 296 | Glycogen storage disease type II | 2.4% |
| 297 | Hydrops Fetalis | 2.4% |
| 298 | Basal Cell Nevus Syndrome | 2.4% |
| 299 | Facial Nerve Injuries | 2.4% |
| 300 | Corneal Perforation | 2.3% |
| 301 | Poland Syndrome | 2.3% |
| 302 | Arthrogryposis | 2.3% |
| 303 | Choanal Atresia | 2.3% |
| 304 | Mucopolysaccharidosis III | 2.3% |
| 305 | Tracheobronchomegaly | 2.3% |
| 306 | Laryngocele | 2.3% |
| 307 | Jaw Abnormalities | 2.3% |
| 308 | Cleft Palate | 2.3% |
| 309 | Choledochal Cyst | 2.3% |
| 310 | Duane Retraction Syndrome | 2.3% |
| 311 | Hermaphroditism | 2.3% |
| 312 | Disorders of Sex Development | 2.3% |
| 313 | Cryptorchidism | 2.3% |
| 314 | Porphyrias, Hepatic | 2.3% |
| 315 | Hypospadias | 2.3% |
| 316 | Ataxia Telangiectasia | 2.3% |
| 317 | Central Nervous System Cysts | 2.3% |
| 318 | Dandy-Walker Syndrome | 2.2% |
| 319 | Peutz-Jeghers Syndrome | 2.2% |
| 320 | Myotonia Congenita | 2.2% |
| 321 | Thrombasthenia | 2.2% |
| 322 | Antithrombin III Deficiency | 2.2% |
| 323 | Protein C Deficiency | 2.2% |
| 324 | Brain Diseases, Metabolic, Inborn | 2.2% |
| 325 | Afibrinogenemia | 2.2% |
| 326 | Dystonia Musculorum Deformans | 2.2% |
| 327 | Factor VII Deficiency | 2.2% |
| 328 | Factor X Deficiency | 2.2% |
| 329 | Factor XII Deficiency | 2.2% |
| 330 | Hemophilia A | 2.2% |
| 331 | POEMS Syndrome | 2.2% |
| 332 | Activated Protein C Resistance | 2.2% |
| 333 | Factor II deficiency | 2.2% |
| 334 | Factor VIII Deficiency | 2.2% |
| 335 | Factor V deficiency | 2.2% |
| 336 | Factor XI Deficiency | 2.2% |
| 337 | Hypoprothrombinemias | 2.2% |
| 338 | Fanconi Anemia | 2.2% |
| 339 | Lafora Disease | 2.2% |
| 340 | Unverricht-Lundborg Syndrome | 2.2% |
| 341 | Anemia, Diamond-Blackfan | 2.2% |
| 342 | Optic Atrophy, Hereditary, Leber | 2.2% |
| 343 | Hyperphosphaturia | 2.2% |
| 344 | Canavan Disease | 2.1% |
| 345 | Alexander Disease | 2.1% |
| 346 | Dermal Sinus | 2.1% |
| 347 | Spina Bifida Cystica | 2.1% |
| 348 | Spina Bifida Occulta | 2.1% |
| 349 | Lissencephaly | 2.1% |
| 350 | Polymicrogyria | 2.1% |
| 351 | Pachygyria | 2.1% |
| 352 | Schizencephaly | 2.1% |
| 353 | Periventricular Nodular Heterotopia | 2.1% |
| 354 | Glycogen Storage Disease Type I | 2.1% |
| 355 | Glycogen Storage Disease Type V | 2.1% |
| 356 | Hematoma, Subdural | 2% |
| 357 | Hematoma, Epidural, Cranial | 2% |
| 358 | Aortic coarctation | 2% |
| 359 | Cor Triatriatum | 2% |
| 360 | Coronary Vessel Anomalies | 2% |
| 361 | Dental Enamel Hypoplasia | 2% |
| 362 | Patent ductus arteriosus | 2% |
| 363 | Ebstein Anomaly | 2% |
| 364 | Heart Septal Defects | 2% |
| 365 | Hypodontia | 2% |
| 366 | Macrostomia | 2% |
| 367 | Meningocele | 2% |
| 368 | Microstomia | 2% |
| 369 | Tetralogy of Fallot | 2% |
| 370 | Transposition of Great Vessels | 2% |
| 371 | Hypoplastic Left Heart Syndrome | 2% |
| 372 | May-Thurner Syndrome | 2% |
| 373 | Encephalocele | 2% |
| 374 | Homocystinuria | 2% |
| 375 | Craniofacial Dysostosis | 2% |
| 376 | Leigh Disease | 2% |
| 377 | Hypolipoproteinemias | 2% |
| 378 | Papillon-Lefevre Disease | 2% |
| 379 | Wolff-Parkinson-White Syndrome | 2% |
| 380 | Hyperlipidemia, Familial Combined | 2% |
| 381 | Multiple Endocrine Neoplasia | 2% |
| 382 | Laryngomalacia | 2% |
| 383 | Hyperlipoproteinemia Type III | 2% |
| 384 | Gaucher Disease | 2% |
| 385 | Pectus carinatum | 2% |
| 386 | Micrognathism | 1.9% |
| 387 | Pierre Robin Syndrome | 1.9% |
| 388 | Bladder Exstrophy | 1.9% |
| 389 | Congenital Hypothyroidism | 1.9% |
| 390 | Epispadias | 1.9% |
| 391 | Dermatitis, Atopic | 1.9% |
| 392 | Multicystic Dysplastic Kidney | 1.9% |
| 393 | Hematoma, Subdural, Intracranial | 1.8% |
| 394 | Hematoma, Subdural, Chronic | 1.8% |
| 395 | Hematoma, Subdural, Acute | 1.8% |
| 396 | Carbamoyl-Phosphate Synthase I Deficiency Disease | 1.8% |
| 397 | Subarachnoid Hemorrhage, Traumatic | 1.8% |
| 398 | Carotid Artery, Internal, Dissection | 1.8% |
| 399 | Tay-Sachs Disease | 1.8% |
| 400 | Retrognathia | 1.7% |
| 401 | Niemann-Pick Disease, Type C | 1.7% |
| 402 | Familial Periodic Paralysis | 1.7% |
| 403 | Behcet Syndrome | 1.7% |
| 404 | Long QT Syndrome | 1.7% |
| 405 | Platybasia | 1.7% |
| 406 | Tricuspid Atresia | 1.7% |
| 407 | Arrhythmogenic Right Ventricular Dysplasia | 1.7% |
| 408 | Gonadal Dysgenesis | 1.7% |
| 409 | Bronchomalacia | 1.7% |
| 410 | Adrenogenital Syndrome | 1.7% |
| 411 | Tracheomalacia | 1.7% |
| 412 | Ovotesticular Disorders of Sex Development | 1.7% |
| 413 | Lactose Intolerance | 1.7% |
| 414 | Variegate Porphyria | 1.7% |
| 415 | Acute intermittent porphyria | 1.7% |
| 416 | Porphyria Cutanea Tarda | 1.7% |
| 417 | Hyperhomocysteinemia | 1.7% |
| 418 | Aortopulmonary Septal Defect | 1.7% |
| 419 | Double Outlet Right Ventricle | 1.7% |
| 420 | Endocardial Cushion Defects | 1.7% |
| 421 | Myocardial bridging | 1.7% |
| 422 | Aorticopulmonary Septal Defect | 1.7% |
| 423 | Renal Aminoacidurias | 1.6% |
| 424 | Fanconi Syndrome | 1.6% |
| 425 | Pseudohypoaldosteronism | 1.6% |
| 426 | Liddle Syndrome | 1.6% |
| 427 | Hypoalphalipoproteinemias | 1.6% |
| 428 | Hyperlipoproteinemia Type IV | 1.6% |
| 429 | Hyperlipoproteinemia Type V | 1.6% |
| 430 | Hyperandrogenism | 1.6% |
| 431 | Prognathism | 1.6% |
| 432 | Huntington Disease | 1.5% |
| 433 | Truncus Arteriosus, Persistent | 1.5% |
| 434 | Goldenhar Syndrome | 1.5% |
| 435 | Gout | 1.4% |
| 436 | Multiple Endocrine Neoplasia Type 1 | 1.4% |
| 437 | Pseudohypoparathyroidism | 1.4% |
| 438 | Friedreich Ataxia | 1.4% |
| 439 | Renal tubular acidosis | 1.4% |
| 440 | Hypokalemic periodic paralysis | 1.4% |
| 441 | Mandibulofacial Dysostosis | 1.4% |
| 442 | Romano-Ward Syndrome | 1.4% |
| 443 | Cystinuria | 1.4% |
| 444 | Nephroblastoma | 1.3% |
| 445 | Denys-Drash Syndrome | 1.3% |
| 446 | Talipes | 1.2% |
| 447 | Adenomatous Polyposis Coli | 1.2% |
| 448 | Arthritis, Gouty | 1.2% |
| 449 | Congenital clubfoot | 1.2% |
| 450 | Vertical Talus | 1.2% |
| 451 | Familial Hypophosphatemic Rickets | 1.1% |
| 452 | Glycosuria, Renal | 1.1% |
| 453 | Arteriovenous fistula | 1% |
| 454 | MELAS Syndrome | 0.9% |