| Label | Id | |
|---|---|---|
| holoprosencephaly 1 | 9349.0 | |
| ovarian dysgenesis 2 | 10349.0 | |
| obsolete Charcot-Marie-Tooth disease type 1 | 349.0 | |
| pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities | 8349.0 | |
| progressive cavitating leukoencephalopathy | 15349.0 | |
| acute motor axonal neuropathy | 20349.0 | |
| pontocerebellar hypoplasia type 10 | 14349.0 | |
| ALG11-CDG | 13349.0 | |
| retina lymphoma | 4349.0 | |
| MAN1B1-CDG | 18349.0 |