| Sort by Name
Show Adult Diagnoses
| Sort by Prevalence |
|
| Attention Deficit Hyperactivity Disorder |
1/11 |
227 |
| Asthma (pediatric) |
1/20 |
125 |
| Depression |
1/20 |
125 |
| Intellectual Disability / Mental Retardation |
1/40 |
63 |
| Tourette syndrome |
1/100 |
25 |
| Autism Spectrum Disorder |
1/152 |
16 |
| Congenital Heart Disease |
1/154 |
16 |
| Seizure Disorder |
1/286 |
9 |
| Pyloric Stenosis |
1/300 |
8 |
| Hearing Impairment |
1/333 |
8 |
| Visual Impairment |
1/333 |
8 |
| Congenital Heart Defects, all (1/200 - 1/500) |
1/350 |
7 |
| Arthritis |
1/455 |
5 |
| Rheumatic Heart Disease |
1/455 |
5 |
| Hydrocephalus |
1/500 |
5 |
| Familial Hypercholesterolemia (heterozygote) |
1/500 |
5 |
| Cerebral Palsy |
1/500 |
5 |
| Diabetes Mellitus, Type I, in children |
1/556 |
4 |
| Down Syndrome |
1/660 |
4 |
| Cleft Lip/Palate |
1/667 |
4 |
| Club Foot |
1/1000 |
3 |
| Ventricular Septal Defect |
1/1091 |
2 |
| Celiac Disease |
1/1111 |
2 |
| Traumatic Brain Injury |
1/1378 |
2 |
| Coarctation of the Aorta (Utah data) |
1/1429 |
2 |
| Blindness |
1/1667 |
1 |
| Atrial Septal Defect |
1/1667 |
1 |
| Patent Ductus Arteriosus |
1/1667 |
1 |
| Neural Tube Defects |
1/1724 |
1 |
| Klinefelter Syndrome (1/1000 males) |
1/2000 |
1 |
| Coarctation of the Aorta |
1/2083 |
1 |
| Pulmonary Valve Stenosis |
1/2083 |
1 |
| Sickle Cell Disease |
1/2174 |
1 |
| Aortic Valve Stenosis |
1/2273 |
1 |
| Juvenile Rheumatoid Arthritis |
1/2500 |
1 |
| Tetralogy of Fallot |
1/2564 |
1 |
| Hypoplastic Left Heart Syndrome (Utah Data) |
1/2632 |
1 |
| Fragile X syndrome (males>females) |
1/2703 |
1 |
| Spinal Cord Injury |
1/2861 |
1 |
| d-Transposition of the Great Arteries |
1/3125 |
1 |
| Cystic Fibrosis |
1/3500 |
1 |
| Neurofibromatosis, Type I |
1/3500 |
1 |
| Sickle Cell Anemia |
1/3571 |
1 |
| Congenital Hypothyroidism |
1/3700 |
1 |
| Growth Hormone Deficiency |
1/4000 |
1 |
| Hemochromatosis (hereditary, symptomatic) |
1/5000 |
1 |
| Hirschsprung's Disease |
1/5000 |
1 |
| Trisomy 18 |
1/6000 |
0.4 |
| Spinal Muscle Atrophy (SMA) |
1/6000 |
0.4 |
| Hypoplastic Left Ventricle |
1/6250 |
0.4 |
| Hypoplastic Right Ventricle |
1/6250 |
0.4 |
| Hemophilia |
1/6667 |
0.4 |
| Duchenne Muscular Dystrophy (1/3500 males) |
1/7000 |
0.4 |
| Cancer (childhood, all types) |
1/7353 |
0.3 |
| Osteogenesis Imperfecta (1/5000 - 1/10000) |
1/7500 |
0.3 |
| Truncus Arteriosus |
1/8333 |
0.3 |
| Tricuspid Atresia |
1/8333 |
0.3 |
| Single Ventricle |
1/8333 |
0.3 |
| Double Outlet Right Ventricle |
1/8333 |
0.3 |
| Total Anomalous Pulmonary Venous Return |
1/8333 |
0.3 |
| Romano-Ward Syndrome |
1/10000 |
0.3 |
| Choanal Atresia |
1/10000 |
0.3 |
| Wilms Tumor |
1/10000 |
0.3 |
| Trisomy 13 |
1/10000 |
0.3 |
| Deafness |
1/10000 |
0.3 |
| Glaucoma |
1/10000 |
0.3 |
| Phenylketonuria |
1/12000 |
0.2 |
| Chronic Renal Failure |
1/12500 |
0.2 |
| Prader Willi Syndrome |
1/13500 |
0.2 |
| Congenital Adrenal Hyperplasia |
1/15000 |
0.2 |
| Truncus Arteriosus (Utah data) |
1/16667 |
0.1 |
| Muscular Dystrophy |
1/16667 |
0.1 |
| Retinoblastoma |
1/18000 |
0.1 |
| Huntington Disease (in whites) |
1/20000 |
0.1 |
| Polycystic Kidney Disease, autsomal recessive |
1/20000 |
0.1 |
| Primary Ciliary Dyskinesia (immotile cilia) |
1/20000 |
0.1 |
| Rett Syndrome |
1/20000 |
0.1 |
| Glycogen Metabolism/Storage Diseases |
1/20000 |
0.1 |
| Acute Lymphoblastic Leukemia |
1/30000 |
0.1 |
| Ataxia-Telangiectasia |
1/90000 |
0 |
| Hurler syndrome (Mucopolysaccharidosis type I) |
1/100000 |
0 |
| Chronic Granulomatous Disease |
1/500000 |
0 |
| Myasthenia Gravis |
1/500000 |
0 |
| Familial Hypercholesterolemia (homozygote) |
1/1000000 |
0 |
