Simplifying Science™
| A | From abdominal wall anomaly to AVM, pulmonary |
| B | From bands, anomalous congenital to BWS |
| C | From Caffey's disease to cystic kidney disease, medullary |
| D | From 17-20-desmolase deficiency, testicular to dysplasia, renal-hepatic-pancreatic |
| E | From E3, trisomy to exomphalos-macroglossia-gigantism syndrome |
| F | From face bone anomaly, skull and to functional colon disorder, congenital |
| G | From gallbladder, bile duct, or liver anomaly to great vessels, transposition of |
| H | From heart anomaly to hyptonia-obesity-prominent incisors syndrome |
| I | From ichthyosiform erythroderma with leukocyte vacuolation to inversus, unspecified, situs |
| J | From jejunal absence, congenital to juvenile nephrophthisis, familial |
| K | From Kabuki make-up syndrome to Klinefelter's syndrome |
| L | From Lange syndrome, Brachman-de to lymphedema, unspecified, hereditary |
| M | From macroglossia to myelomeningocele |
| N | From nail syndrome, yellow to nutcracker syndrome, renal |
| O | From obesity-hypotonia syndrome to ovotesticular DSD |
| P | From palate, cleft to pyloric stenosis, infantile hypertrophic |
| R | From recessive dyskeratosis congenita, autosomal to RTS |
| S | From sclerosis complex, tuberous to system anomaly, urinary |
| T | From TAPVR to Type III, endochondromatosis Spranger |
| U | From undescended or retractile testicle to uterine anomaly |
| V | From vacuolation, ichthyosiform erythroderma with leukocyte to VSD |
| W | From wall anomaly, abdominal to Wolf-Hirschhorn syndrome |
| X | From 46 XX disorder of sexual development to XYY syndrome, 47 |
| Y | From Y, polysomy to YY syndrome |
| Z | From Zellweger syndrome to ZWS |
