| 1 | Job Syndrome | 38.2% |
| 2 | Wiskott-Aldrich Syndrome | 28.3% |
| 3 | Pelger-Huet Anomaly | 26.2% |
| 4 | Lymphopenia | 21.3% |
| 5 | Muscular Dystrophy, Duchenne | 18.7% |
| 6 | Aicardi's syndrome | 18.3% |
| 7 | Anemia, Sickle Cell | 17.6% |
| 8 | Thalassemia | 17.6% |
| 9 | Transfusion Reaction | 17.5% |
| 10 | Hypotensive Transfusion Reaction | 17.5% |
| 11 | Eosinophilia | 17.4% |
| 12 | Leukopenia | 17.4% |
| 13 | Leukostasis | 17.4% |
| 14 | Fragile X Syndrome | 17% |
| 15 | Thrombasthenia | 17% |
| 16 | Antithrombin III Deficiency | 17% |
| 17 | Protein C Deficiency | 17% |
| 18 | Agammaglobulinemia | 16.8% |
| 19 | Rett Syndrome | 16.3% |
| 20 | Afibrinogenemia | 15.5% |
| 21 | Factor VII Deficiency | 15.5% |
| 22 | Factor X Deficiency | 15.5% |
| 23 | Factor XII Deficiency | 15.5% |
| 24 | Hemophilia A | 15.5% |
| 25 | Activated Protein C Resistance | 15.5% |
| 26 | Factor II deficiency | 15.5% |
| 27 | Factor VIII Deficiency | 15.5% |
| 28 | Factor V deficiency | 15.5% |
| 29 | Factor XI Deficiency | 15.5% |
| 30 | Hypoprothrombinemias | 15.5% |
| 31 | Ichthyosis, X-Linked | 15.3% |
| 32 | Autoimmune Lymphoproliferative Syndrome | 15% |
| 33 | Disseminated Intravascular Coagulation | 14.9% |
| 34 | Protein S Deficiency | 14.9% |
| 35 | Leukocytosis | 14.1% |
| 36 | Pleocytosis | 14.1% |
| 37 | Thrombocythemia, Essential | 13.3% |
| 38 | Infectious Mononucleosis | 13.2% |
| 39 | Mucopolysaccharidosis II | 13.2% |
| 40 | Leukemoid Reaction | 13.1% |
| 41 | Sickle Cell Trait | 12.9% |
| 42 | Anemia | 12.6% |
| 43 | Blood Coagulation Disorders | 12.6% |
| 44 | Blood Platelet Disorders | 12.6% |
| 45 | Bone Marrow Diseases | 12.6% |
| 46 | Hemorrhagic Disorders | 12.6% |
| 47 | Methemoglobinemia | 12.6% |
| 48 | Pancytopenia | 12.6% |
| 49 | Polycythemia | 12.6% |
| 50 | Sulfhemoglobinemia | 12.6% |
| 51 | Thrombophilia | 12.6% |
| 52 | Erythrocytosis | 12.6% |
| 53 | Neoplastic Syndromes, Hereditary | 12.6% |
| 54 | Anemia, Diamond-Blackfan | 12.6% |
| 55 | CHARGE Syndrome | 12.3% |
| 56 | Multiple Epiphyseal Dysplasia | 12.1% |
| 57 | Osteochondrodysplasias | 12.1% |
| 58 | Werner Syndrome | 12.1% |
| 59 | Myasthenic Syndromes, Congenital | 12.1% |
| 60 | Ataxia Telangiectasia | 12.1% |
| 61 | Menkes Kinky Hair Syndrome | 12% |
| 62 | Cystic Fibrosis | 11.8% |
| 63 | Agranulocytosis | 11.5% |
| 64 | Lymphocytosis | 11.5% |
| 65 | Hypereosinophilic syndrome | 11.5% |
| 66 | Beckwith-Wiedemann Syndrome | 11% |
| 67 | Wolf-Hirschhorn Syndrome | 11% |
| 68 | Albinism | 10.9% |
| 69 | Nail-Patella Syndrome | 10.6% |
| 70 | Dwarfism | 10.4% |
| 71 | Classical Lissencephalies and Subcortical Band Heterotopias | 10.4% |
| 72 | Cockayne Syndrome | 10.3% |
| 73 | Fabry Disease | 10.3% |
| 74 | Hydrops Fetalis | 10.2% |
| 75 | Acute Chest Syndrome | 10.2% |
| 76 | Pregnancy Complications, Hematologic | 10.2% |
| 77 | Hematologic Neoplasms | 10.2% |
| 78 | Anemia, Neonatal | 10.1% |
| 79 | Paraproteinemias | 10.1% |
| 80 | HIV Infections | 10% |
| 81 | Muscular Dystrophy | 10% |
| 82 | Osteogenesis Imperfecta | 10% |
| 83 | Bone Marrow Neoplasms | 9.9% |
| 84 | Familial Mediterranean Fever | 9.9% |
| 85 | Thrombocytosis | 9.9% |
| 86 | Vitamin K Deficiency | 9.9% |
| 87 | Fanconi Anemia | 9.8% |
| 88 | Alstrom Syndrome | 9.8% |
| 89 | Angioedemas, Hereditary | 9.7% |
| 90 | Autoimmune thrombocytopenia | 9.6% |
| 91 | Immune thrombocytopenic purpura | 9.6% |
| 92 | Smith-Magenis syndrome | 9.6% |
| 93 | Cri-du-Chat Syndrome | 9.4% |
| 94 | Down Syndrome | 9.4% |
| 95 | Trisomy 21 | 9.4% |
| 96 | Adrenoleukodystrophy | 9.4% |
| 97 | Monoclonal Gammopathy of Undetermined Significance | 9.4% |
| 98 | Autoimmune Diseases | 8.7% |
| 99 | Hypersensitivity | 8.7% |
| 100 | Immunoproliferative Disorders | 8.7% |
| 101 | Deformity | 8.7% |
| 102 | Immune reconstitution syndrome | 8.7% |
| 103 | Immune Reconstitution Inflammatory Syndrome | 8.7% |
| 104 | Kartagener Syndrome | 8.7% |
| 105 | Holoprosencephaly | 8.6% |
| 106 | Neutropenia | 8.6% |
| 107 | Thrombocytopenic purpura | 8.6% |
| 108 | Hypergammaglobulinemia | 8.5% |
| 109 | Marfan Syndrome | 8.4% |
| 110 | Polycythemia Vera | 8.4% |
| 111 | Transfusion-Related Acute Lung Injury | 8.3% |
| 112 | Ectodermal Dysplasia | 8.3% |
| 113 | Aplasia Cutis Congenita | 8.3% |
| 114 | Prader-Willi Syndrome | 8.2% |
| 115 | Smith-Lemli-Opitz Syndrome | 8% |
| 116 | Neuronal Ceroid-Lipofuscinoses | 8% |
| 117 | Amino Acid Metabolism, Inborn Errors | 7.9% |
| 118 | Carbohydrate Metabolism, Inborn Errors | 7.9% |
| 119 | Metal Metabolism, Inborn Errors | 7.9% |
| 120 | Progeria | 7.9% |
| 121 | Lysosomal Storage Diseases | 7.9% |
| 122 | Cytochrome-c Oxidase Deficiency | 7.9% |
| 123 | Peroxisomal Disorders | 7.9% |
| 124 | HTLV-I Infections | 7.9% |
| 125 | Myotonic Dystrophy | 7.9% |
| 126 | Hemoglobinuria, Paroxysmal | 7.8% |
| 127 | Lymphatic Diseases | 7.8% |
| 128 | Eosinophilia-Myalgia Syndrome | 7.8% |
| 129 | Rubinstein-Taybi Syndrome | 7.6% |
| 130 | Cryoglobulinemia | 7.5% |
| 131 | Primary Ciliary Dyskinesia | 7.5% |
| 132 | Polycystic Kidney Diseases | 7.5% |
| 133 | Williams Syndrome | 7.5% |
| 134 | Lymphoproliferative Disorders | 7.5% |
| 135 | Lymphatic Abnormalities | 7.5% |
| 136 | Kallmann Syndrome | 7.5% |
| 137 | Tuberous Sclerosis | 7.5% |
| 138 | Anemia, Hemolytic | 7.4% |
| 139 | Anemia, Macrocytic | 7.4% |
| 140 | Hypoproteinemia | 7.4% |
| 141 | Thrombocytopenia | 7.4% |
| 142 | MYELODYSPLASTIC SYNDROME | 7.4% |
| 143 | Pseudoxanthoma Elasticum | 7.3% |
| 144 | Multiple Myeloma | 7.3% |
| 145 | Sjogren-Larsson Syndrome | 7.2% |
| 146 | Heavy Chain Disease | 7.1% |
| 147 | Febrile Neutropenia | 7.1% |
| 148 | Kernicterus | 7% |
| 149 | Hepatolenticular Degeneration | 7% |
| 150 | Fetal Diseases | 7% |
| 151 | Pulmonary Eosinophilia | 7% |
| 152 | Purpura, Thrombotic Thrombocytopenic | 7% |
| 153 | Eosinophilic Pneumonia | 7% |
| 154 | Waldenstrom Macroglobulinemia | 7% |
| 155 | Refsum Disease | 6.9% |
| 156 | Amyloid Neuropathies, Familial | 6.8% |
| 157 | Retinal Dysplasia | 6.8% |
| 158 | Aniridia | 6.8% |
| 159 | Cutis Laxa | 6.7% |
| 160 | Retinitis Pigmentosa | 6.7% |
| 161 | Pigmentary retinopathy | 6.7% |
| 162 | Dermatitis, Atopic | 6.6% |
| 163 | Epidermolysis Bullosa | 6.6% |
| 164 | Porokeratosis | 6.6% |
| 165 | Keratoderma, Palmoplantar | 6.6% |
| 166 | Eosinophilic Granuloma | 6.6% |
| 167 | POEMS Syndrome | 6.6% |
| 168 | Glycogen storage disease type II | 6.6% |
| 169 | HIV Seropositivity | 6.5% |
| 170 | Welander Distal Myopathy | 6.5% |
| 171 | Galactosemias | 6.5% |
| 172 | Urea Cycle Disorders, Inborn | 6.5% |
| 173 | Tyrosinemias | 6.5% |
| 174 | Mucopolysaccharidosis III | 6% |
| 175 | Alkaptonuria | 5.9% |
| 176 | Glycogen Storage Disease | 5.9% |
| 177 | Hypophosphatasia | 5.9% |
| 178 | Propionic acidemia | 5.9% |
| 179 | Dihydropyrimidine Dehydrogenase Deficiency | 5.9% |
| 180 | Cystinosis | 5.9% |
| 181 | Optic Atrophy, Hereditary, Leber | 5.9% |
| 182 | Hyperphosphaturia | 5.8% |
| 183 | Duane Retraction Syndrome | 5.8% |
| 184 | Canavan Disease | 5.8% |
| 185 | Alexander Disease | 5.8% |
| 186 | Porphyrias, Hepatic | 5.7% |
| 187 | Acquired Immunodeficiency Syndrome | 5.7% |
| 188 | AIDS related complex | 5.7% |
| 189 | Peutz-Jeghers Syndrome | 5.7% |
| 190 | Myotonia Congenita | 5.7% |
| 191 | Brain Diseases, Metabolic, Inborn | 5.7% |
| 192 | Dystonia Musculorum Deformans | 5.6% |
| 193 | Glomerulonephritis, Membranoproliferative | 5.6% |
| 194 | Lafora Disease | 5.6% |
| 195 | Unverricht-Lundborg Syndrome | 5.6% |
| 196 | Polycystic Kidney, Autosomal Dominant | 5.5% |
| 197 | Zellweger Syndrome | 5.5% |
| 198 | Lymphangiectasis, Intestinal | 5.5% |
| 199 | Homocystinuria | 5.4% |
| 200 | Gaucher Disease | 5.4% |
| 201 | Leigh Disease | 5.3% |
| 202 | Hyperkeratosis, Epidermolytic | 5.2% |
| 203 | Meconium Aspiration Syndrome | 5.1% |
| 204 | Multiple Endocrine Neoplasia | 5.1% |
| 205 | Abdominal Cramps | 5% |
| 206 | Abnormalities, Drug-Induced | 5% |
| 207 | Amniotic Band Syndrome | 5% |
| 208 | Asphyxia Neonatorum | 5% |
| 209 | Immune Complex Diseases | 5% |
| 210 | Infant, Premature, Diseases | 5% |
| 211 | Situs Inversus | 5% |
| 212 | Antiphospholipid Syndrome | 5% |
| 213 | Infantile Colic | 5% |
| 214 | Latex allergy | 5% |
| 215 | Niemann-Pick Disease, Type C | 5% |
| 216 | AIDS-Related Opportunistic Infections | 5% |
| 217 | Congenital Hypothyroidism | 5% |
| 218 | Ecchymosis | 5% |
| 219 | Petechiae | 5% |
| 220 | Purpura | 5% |
| 221 | HIV Wasting Syndrome | 4.9% |
| 222 | Primary Myelofibrosis | 4.9% |
| 223 | Anemia, Megaloblastic | 4.9% |
| 224 | Myelofibrosis | 4.9% |
| 225 | Myeloid Metaplasia | 4.9% |
| 226 | Hypoalbuminemia | 4.9% |
| 227 | bone marrow fibrosis | 4.9% |
| 228 | Thrombotic Microangiopathies | 4.9% |
| 229 | AIDS Dementia Complex | 4.9% |
| 230 | AIDS-Associated Nephropathy | 4.9% |
| 231 | Tay-Sachs Disease | 4.9% |
| 232 | Purpura, Hyperglobulinemic | 4.9% |
| 233 | Hypolipoproteinemias | 4.9% |
| 234 | Papillon-Lefevre Disease | 4.9% |
| 235 | Charcot-Marie-Tooth Disease | 4.9% |
| 236 | Antley-Bixler Syndrome Phenotype | 4.9% |
| 237 | Hyperlipidemia, Familial Combined | 4.9% |
| 238 | Hyperlipoproteinemia Type III | 4.9% |
| 239 | Glycogen Storage Disease Type I | 4.9% |
| 240 | Glycogen Storage Disease Type V | 4.9% |
| 241 | Xeroderma Pigmentosum | 4.9% |
| 242 | Hemolytic-Uremic Syndrome | 4.9% |
| 243 | Carbamoyl-Phosphate Synthase I Deficiency Disease | 4.8% |
| 244 | Xeroderma | 4.8% |
| 245 | Mobius Syndrome | 4.8% |
| 246 | Tumor Lysis Syndrome | 4.6% |
| 247 | Behcet Syndrome | 4.4% |
| 248 | Basal Cell Nevus Syndrome | 4.4% |
| 249 | HIV-Associated Lipodystrophy Syndrome | 4.3% |
| 250 | Familial Periodic Paralysis | 4.3% |
| 251 | Lactose Intolerance | 4.2% |
| 252 | Variegate Porphyria | 4.2% |
| 253 | Acute intermittent porphyria | 4.2% |
| 254 | Porphyria Cutanea Tarda | 4.2% |
| 255 | Adenitis | 4.2% |
| 256 | Histiocytosis | 4.2% |
| 257 | Lymphadenitis | 4.2% |
| 258 | Lymphangitis | 4.2% |
| 259 | Lymphedema | 4.2% |
| 260 | Splenic Diseases | 4.2% |
| 261 | Thymus Hyperplasia | 4.2% |
| 262 | Pseudolymphoma | 4.2% |
| 263 | Lymphadenopathy | 4.2% |
| 264 | Eye Abnormalities | 4.2% |
| 265 | Cardiovascular Abnormalities | 4.2% |
| 266 | Environmental Illness | 4.2% |
| 267 | Hyperhomocysteinemia | 4.2% |
| 268 | Renal Aminoacidurias | 4.2% |
| 269 | Fanconi Syndrome | 4.2% |
| 270 | Pseudohypoaldosteronism | 4.2% |
| 271 | Liddle Syndrome | 4.2% |
| 272 | Sezary Syndrome | 4.2% |
| 273 | Hyperlipoproteinemia Type IV | 4.2% |
| 274 | Hyperlipoproteinemia Type V | 4.2% |
| 275 | Lupus Erythematosus, Systemic | 4.1% |
| 276 | Skin Abnormalities | 4.1% |
| 277 | Overlap syndrome | 4.1% |
| 278 | Congenital Microtia | 4.1% |
| 279 | Waterhouse-Friderichsen Syndrome | 4% |
| 280 | Klinefelter Syndrome | 4% |
| 281 | Hypoalphalipoproteinemias | 4% |
| 282 | Addison Disease | 4% |
| 283 | Pemphigus | 4% |
| 284 | Persistent Fetal Circulation Syndrome | 4% |
| 285 | Autoimmune thyroiditis | 4% |
| 286 | Primary Adrenal Insufficiency | 4% |
| 287 | Congenital diaphragmatic hernia | 4% |
| 288 | Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis | 4% |
| 289 | Autoimmune hepatitis | 4% |
| 290 | Umbilical hernia | 4% |
| 291 | Huntington Disease | 3.9% |
| 292 | Leukemia, Myelomonocytic, Chronic | 3.9% |
| 293 | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative | 3.9% |
| 294 | Lymphoma | 3.9% |
| 295 | Anencephaly | 3.8% |
| 296 | Atypical Hemolytic Uremic Syndrome | 3.8% |
| 297 | Primary amyloidosis | 3.8% |
| 298 | Gout | 3.7% |
| 299 | Multiple Endocrine Neoplasia Type 1 | 3.7% |
| 300 | Pseudohypoparathyroidism | 3.7% |
| 301 | Friedreich Ataxia | 3.7% |
| 302 | Renal tubular acidosis | 3.7% |
| 303 | Turner Syndrome | 3.6% |
| 304 | Nephroblastoma | 3.6% |
| 305 | Urogenital Abnormalities | 3.5% |
| 306 | Hypokalemic periodic paralysis | 3.5% |
| 307 | Cystinuria | 3.5% |
| 308 | Neonatal Abstinence Syndrome | 3.4% |
| 309 | Lymphocele | 3.4% |
| 310 | Latent Autoimmune Diabetes in Adults | 3.4% |
| 311 | Thymus Neoplasms | 3.4% |
| 312 | Dermatitis Herpetiformis | 3.4% |
| 313 | Fetal Growth Retardation | 3.4% |
| 314 | Kounis Syndrome | 3.4% |
| 315 | Fetal Hypoxia | 3.3% |
| 316 | Maxillofacial Abnormalities | 3.3% |
| 317 | Congenital nystagmus | 3.3% |
| 318 | Dural Arteriovenous Fistula | 3.3% |
| 319 | Fetal Alcohol Spectrum Disorders | 3.3% |
| 320 | Asthma, Aspirin-Induced | 3.3% |
| 321 | anaphylaxis | 3.3% |
| 322 | Food Allergy | 3.3% |
| 323 | Prune Belly Syndrome | 3.3% |
| 324 | Toxoplasmosis, Congenital | 3.3% |
| 325 | Twins, Conjoined | 3.3% |
| 326 | Waardenburg Syndrome | 3.3% |
| 327 | Anaphylactic shock | 3.3% |
| 328 | Dextrocardia | 3.3% |
| 329 | Shwartzman Phenomenon | 3.3% |
| 330 | Syphilis, Congenital | 3.3% |
| 331 | Hemangioma, Cavernous | 3.3% |
| 332 | Serum Sickness | 3.3% |
| 333 | Scurvy | 3.3% |
| 334 | Purpura Fulminans | 3.3% |
| 335 | Adenomatous Polyposis Coli | 3.2% |
| 336 | Familial Hypophosphatemic Rickets | 3.2% |
| 337 | Arthritis, Gouty | 3% |
| 338 | Leukemia, Myeloid, Chronic-Phase | 2.9% |
| 339 | Anemia, Pernicious | 2.9% |
| 340 | Glycosuria, Renal | 2.9% |
| 341 | Rheumatoid Arthritis | 2.9% |
| 342 | Juvenile arthritis | 2.9% |
| 343 | Graves Disease | 2.9% |
| 344 | Congenital Hyperinsulinism | 2.9% |
| 345 | Chorioamnionitis | 2.9% |
| 346 | Anti-Glomerular Basement Membrane Disease | 2.8% |
| 347 | Mucocutaneous Lymph Node Syndrome | 2.8% |
| 348 | Respiratory Hypersensitivity | 2.8% |
| 349 | Hodgkin Disease | 2.7% |
| 350 | Lymphoma, Non-Hodgkin | 2.7% |
| 351 | Leukemia, T-Cell | 2.7% |
| 352 | Leukemia, B-Cell | 2.7% |
| 353 | Anophthalmos | 2.7% |
| 354 | Anus, Imperforate | 2.7% |
| 355 | Hydranencephaly | 2.7% |
| 356 | Microphthalmos | 2.7% |
| 357 | Neural Tube Defects | 2.7% |
| 358 | Paralysis, Obstetric | 2.7% |
| 359 | Retinopathy of Prematurity | 2.7% |
| 360 | Sick Building Syndrome | 2.7% |
| 361 | Tethered Cord Syndrome | 2.7% |
| 362 | Iniencephaly | 2.7% |
| 363 | Craniorachischisis | 2.7% |
| 364 | Limb Deformities, Congenital | 2.7% |
| 365 | Multiple Chemical Sensitivity | 2.7% |
| 366 | Exencephaly | 2.7% |
| 367 | Septo-Optic Dysplasia | 2.7% |
| 368 | Craniofacial Abnormalities | 2.7% |
| 369 | Cortical Dysplasia | 2.7% |
| 370 | Malformations of Cortical Development | 2.7% |
| 371 | Anorectal Malformations | 2.7% |
| 372 | Bloom Syndrome | 2.6% |
| 373 | Plasmacytoma | 2.6% |
| 374 | Urticaria | 2.6% |
| 375 | Vasculitis, Leukocytoclastic, Cutaneous | 2.6% |
| 376 | Bronchopulmonary Dysplasia | 2.6% |
| 377 | Scimitar Syndrome | 2.6% |
| 378 | Microcephaly | 2.6% |
| 379 | Macrocephaly | 2.6% |
| 380 | Abnormalities, Radiation-Induced | 2.5% |
| 381 | Elephantiasis | 2.5% |
| 382 | Hypersplenism | 2.5% |
| 383 | Sarcoidosis | 2.5% |
| 384 | Elephantiasis Nostras Verrucosa | 2.5% |
| 385 | Acrocephalosyndactylia | 2.5% |
| 386 | Denys-Drash Syndrome | 2.5% |
| 387 | Milk Allergy | 2.5% |
| 388 | Schnitzler Syndrome | 2.5% |
| 389 | Wheat Hypersensitivity | 2.5% |
| 390 | Craniosynostosis | 2.5% |
| 391 | Syndactyly | 2.5% |
| 392 | Brachycephaly | 2.5% |
| 393 | MELAS Syndrome | 2.4% |
| 394 | Composite Lymphoma | 2.3% |
| 395 | Lymphangioleiomyomatosis | 2.3% |
| 396 | Porencephaly | 2.3% |
| 397 | Blepharophimosis | 2.3% |
| 398 | Laryngostenosis | 2.3% |
| 399 | Mouth Abnormalities | 2.3% |
| 400 | Respiratory Distress Syndrome, Newborn | 2.3% |
| 401 | Esophageal Atresia | 2.2% |
| 402 | Intestinal Atresia | 2.2% |
| 403 | Myasthenia Gravis | 2.2% |
| 404 | Uveomeningoencephalitic Syndrome | 2.2% |
| 405 | Horseshoe Kidney | 2.2% |
| 406 | Pectus excavatum | 2.2% |
| 407 | Klippel-Feil Syndrome | 2.2% |
| 408 | Mastocytosis | 2.2% |
| 409 | Gastroschisis | 2.2% |
| 410 | Synostosis | 2.2% |
| 411 | Noonan Syndrome | 2.2% |
| 412 | Acrodermatitis | 2.2% |
| 413 | Drug Eruptions | 2.2% |
| 414 | Gianotti-Crosti Syndrome | 2.2% |
| 415 | Granulomatosis with polyangiitis | 2.2% |
| 416 | Dermatitis, Allergic Contact | 2.2% |
| 417 | Ophthalmia Neonatorum | 2.2% |
| 418 | Myasthenia Gravis, Autoimmune, Experimental | 2.2% |
| 419 | Lymphoma, Follicular | 2.2% |
| 420 | T-Cell Lymphoma | 2.2% |
| 421 | Mantle cell lymphoma | 2.2% |
| 422 | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma | 2.2% |
| 423 | Leukemia, Large Granular Lymphocytic | 2.2% |
| 424 | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma | 2.2% |
| 425 | Cleft Palate | 2.1% |
| 426 | Jaw Abnormalities | 2% |
| 427 | Poland Syndrome | 2% |
| 428 | Granuloma | 2% |
| 429 | Histiocytic Disorders, Malignant | 2% |
| 430 | Splenic Infarction | 2% |
| 431 | Splenic Neoplasms | 2% |
| 432 | Histiocytosis, Langerhans-Cell | 2% |
| 433 | Amelia | 2% |
| 434 | Arachnodactyly | 2% |
| 435 | Ectopia Cordis | 2% |
| 436 | Ectromelia | 2% |
| 437 | Hemimelia | 2% |
| 438 | Meningomyelocele | 2% |
| 439 | Phocomelia | 2% |
| 440 | Sirenomelia | 2% |
| 441 | Spina Bifida | 2% |
| 442 | Polydactyly | 2% |
| 443 | Brachydactyly | 2% |
| 444 | Plagiocephaly | 2% |
| 445 | Lower Extremity Deformities, Congenital | 2% |
| 446 | Upper Extremity Deformities, Congenital | 2% |
| 447 | Single umbilical artery | 2% |
| 448 | Mastocytosis, Systemic | 2% |
| 449 | Arthrogryposis | 2% |
| 450 | Choanal Atresia | 2% |
| 451 | Tracheobronchomegaly | 2% |
| 452 | Laryngocele | 2% |
| 453 | Choledochal Cyst | 1.9% |
| 454 | Hermaphroditism | 1.9% |
| 455 | Disorders of Sex Development | 1.9% |
| 456 | Stiff-Person Syndrome | 1.9% |
| 457 | Polyradiculoneuropathy | 1.9% |
| 458 | Polyradiculoneuritis | 1.9% |
| 459 | Cryptorchidism | 1.9% |
| 460 | Hypospadias | 1.9% |
| 461 | Central Nervous System Cysts | 1.9% |
| 462 | Dandy-Walker Syndrome | 1.9% |
| 463 | Lymphoma, T-Cell, Cutaneous | 1.9% |
| 464 | Lymphoma, AIDS-Related | 1.9% |
| 465 | Enteropathy-Associated T-Cell Lymphoma | 1.9% |
| 466 | Primary Effusion Lymphoma | 1.9% |
| 467 | Felty Syndrome | 1.9% |
| 468 | Leukomalacia, Periventricular | 1.9% |
| 469 | Nesidioblastosis | 1.9% |
| 470 | Lupus Nephritis | 1.9% |
| 471 | Mycosis Fungoides | 1.7% |
| 472 | Lymphomatoid Papulosis | 1.7% |
| 473 | Plasmablastic lymphoma | 1.7% |
| 474 | Micrognathism | 1.7% |
| 475 | Pierre Robin Syndrome | 1.7% |
| 476 | Laryngomalacia | 1.7% |
| 477 | Splenic Rupture | 1.7% |
| 478 | Pectus carinatum | 1.7% |
| 479 | Bladder Exstrophy | 1.7% |
| 480 | Epispadias | 1.7% |
| 481 | Vasculitis, Central Nervous System | 1.7% |
| 482 | Angioedema | 1.7% |
| 483 | Multicystic Dysplastic Kidney | 1.7% |
| 484 | Aortic coarctation | 1.6% |
| 485 | Cor Triatriatum | 1.6% |
| 486 | Coronary Vessel Anomalies | 1.6% |
| 487 | Dental Enamel Hypoplasia | 1.6% |
| 488 | Patent ductus arteriosus | 1.6% |
| 489 | Ebstein Anomaly | 1.6% |
| 490 | Heart Septal Defects | 1.6% |
| 491 | Hyaline Membrane Disease | 1.6% |
| 492 | Hypodontia | 1.6% |
| 493 | Macrostomia | 1.6% |
| 494 | Meningocele | 1.6% |
| 495 | Microstomia | 1.6% |
| 496 | Multiple Sclerosis | 1.6% |
| 497 | Tetralogy of Fallot | 1.6% |
| 498 | Thymoma | 1.6% |
| 499 | Transposition of Great Vessels | 1.6% |
| 500 | Hypoplastic Left Heart Syndrome | 1.6% |
| 501 | May-Thurner Syndrome | 1.6% |
| 502 | Encephalocele | 1.6% |
| 503 | Craniofacial Dysostosis | 1.6% |
| 504 | Leukemia, Plasma Cell | 1.6% |
| 505 | Lymphohistiocytosis, Hemophagocytic | 1.6% |
| 506 | Rheumatoid Vasculitis | 1.6% |
| 507 | Erdheim-Chester Disease | 1.6% |
| 508 | Lymphomatoid Granulomatosis | 1.6% |
| 509 | Neuromyelitis Optica | 1.6% |
| 510 | Wolff-Parkinson-White Syndrome | 1.6% |
| 511 | Acute Generalized Exanthematous Pustulosis | 1.6% |
| 512 | Dermal Sinus | 1.6% |
| 513 | Spina Bifida Cystica | 1.6% |
| 514 | Spina Bifida Occulta | 1.6% |
| 515 | Lissencephaly | 1.6% |
| 516 | Polymicrogyria | 1.6% |
| 517 | Pachygyria | 1.6% |
| 518 | Schizencephaly | 1.6% |
| 519 | Periventricular Nodular Heterotopia | 1.6% |
| 520 | Lupus Vasculitis, Central Nervous System | 1.6% |
| 521 | Leukoencephalitis, Acute Hemorrhagic | 1.6% |
| 522 | Retrognathia | 1.5% |
| 523 | Lambert-Eaton Myasthenic Syndrome | 1.5% |
| 524 | Hyperandrogenism | 1.5% |
| 525 | Sicca Syndrome | 1.5% |
| 526 | Sjogren's Syndrome | 1.5% |
| 527 | Asthma | 1.4% |
| 528 | Burkitt Lymphoma | 1.4% |
| 529 | Long QT Syndrome | 1.4% |
| 530 | Platybasia | 1.4% |
| 531 | Tricuspid Atresia | 1.4% |
| 532 | Arrhythmogenic Right Ventricular Dysplasia | 1.4% |
| 533 | Prognathism | 1.4% |
| 534 | Gonadal Dysgenesis | 1.4% |
| 535 | Bronchomalacia | 1.4% |
| 536 | Adrenogenital Syndrome | 1.4% |
| 537 | Tracheomalacia | 1.4% |
| 538 | Ovotesticular Disorders of Sex Development | 1.4% |
| 539 | Encephalomyelitis, Acute Disseminated | 1.4% |
| 540 | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating | 1.4% |
| 541 | Erythema Nodosum | 1.4% |
| 542 | Neuritis, Autoimmune, Experimental | 1.4% |
| 543 | Dermatitis, Photoallergic | 1.4% |
| 544 | Asthma, Exercise-Induced | 1.4% |
| 545 | Status Asthmaticus | 1.4% |
| 546 | Aortopulmonary Septal Defect | 1.4% |
| 547 | Double Outlet Right Ventricle | 1.4% |
| 548 | Endocardial Cushion Defects | 1.4% |
| 549 | Multiple Sclerosis, Chronic Progressive | 1.4% |
| 550 | Multiple Sclerosis, Relapsing-Remitting | 1.4% |
| 551 | Myocardial bridging | 1.4% |
| 552 | Aorticopulmonary Septal Defect | 1.4% |
| 553 | Malignant histiocytosis | 1.3% |
| 554 | Sarcoidosis, Pulmonary | 1.3% |
| 555 | Histiocytic sarcoma | 1.3% |
| 556 | Aspergillosis, Allergic Bronchopulmonary | 1.2% |
| 557 | Guillain-Barre Syndrome | 1.2% |
| 558 | Hereditary Angioedema Type III | 1.2% |
| 559 | Hereditary Angioedema Types I and II | 1.2% |
| 560 | Truncus Arteriosus, Persistent | 1.2% |
| 561 | Asthma, Occupational | 1.2% |
| 562 | Goldenhar Syndrome | 1.2% |
| 563 | Farmer's Lung | 1.2% |
| 564 | Hay fever | 1.2% |
| 565 | Rhinitis, Allergic, Perennial | 1.2% |
| 566 | Mandibulofacial Dysostosis | 1.2% |
| 567 | Romano-Ward Syndrome | 1.2% |
| 568 | Splenosis | 1.1% |
| 569 | Toxic Epidermal Necrolysis | 1.1% |
| 570 | Stevens-Johnson Syndrome | 1.1% |
| 571 | Talipes | 1.1% |
| 572 | Congenital clubfoot | 1% |
| 573 | Vertical Talus | 1% |
| 574 | Giant Cell Arteritis | 1% |
| 575 | Temporal Arteritis | 1% |
| 576 | Arteriovenous fistula | 0.9% |
| 577 | Myelitis, Transverse | 0.9% |
| 578 | Miller Fisher Syndrome | 0.7% |
