299 |
Pervasive development disorders (e.g. autism) |
317 |
Mild mental retardation |
318 |
Moderate severe and profound mental retardation |
319 |
Unspecified mental retardation |
7580–7583 |
Chromosomal anomalies for which a developmental disability is typically present (e.g. Down syndrome, cri-du-chat syndrome) |
7585 |
Other conditions due to autosomal anomalies |
7588 |
Other conditions due to chromosome anomalies |
7589 |
Conditions due to anomaly of unspecified chromosome |
7595 |
Tuberous sclerosis |
75981 |
Other and unspecified congenital anomalies: Prader–Willi |
75983 |
Other and unspecified congenital anomalies: Fragile X |
75989 |
Other and unspecified congenital anomalies: other (e.g. Menkes disease, Laurence–Moon–Biedl, Rubinstein–Taybi syndrome, etc.) |
76071 |
Foetal alcohol syndrome |
76077 |
Foetal hydantoin syndrome |