| Abbreviations | Meaning |
 | COIF | Congenital Onychodysplasia Of The Index Finger |
| CHILD | Congenital Hemidysplasia With Ichthyosiform Erythroderma And Limb Defects [syndrome] |
| NHS-2 | Second Natural History Study [of Congenital Heart Defects] |
| CHILD SYNDROME | Congenital Hemidysplasia With Ichthyosiform Erythrodermal And Limb Defects |
| FCMD | Fukuyama Congenital Muscular Dystrophy |
| CGFH | Congenital Fibrous Histiocytoma |
| CDG | Congenital Disorders Of Glycosylation |
| CC | Congenital Cataract |
| FCCA | Familial Congenital Cardiac Abnormality |
| CHRPE | Congenital Hypertrophy Of The Retinal Pigment Epithelium |
| MCA | Multiple Congenital Anomaly |
| CRD | Congenital Rubella Deafness |
| CCHS | Congenital Central Hypoventilation Syndrome; Copenhagen City Heart Study |
| CAR | Congenital Articular Rigidity |
| CHS | Congenital Hypoventilation Syndrome |
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