| CUI | Disease | Vocabulary | Name in Vocabulary | Code |
|---|---|---|---|---|
| C0265205 | Robinow Syndrome | DO | Seckel syndrome | 0050569 |
| C0265205 | Robinow Syndrome | DO | Robinow syndrome | 0060254 |
| C0265205 | Robinow Syndrome | DO | Noonan syndrome 1 | 0060578 |
| C0265205 | Robinow Syndrome | DO | Noonan syndrome 2 | 0060580 |
| C0265205 | Robinow Syndrome | DO | Noonan syndrome 3 | 0060581 |
| C0265205 | Robinow Syndrome | DO | Noonan syndrome 4 | 0060582 |
| C0265205 | Robinow Syndrome | DO | Noonan syndrome 5 | 0060583 |
| C0265205 | Robinow Syndrome | DO | Noonan syndrome 6 | 0060584 |
| C0265205 | Robinow Syndrome | DO | Noonan syndrome 7 | 0060585 |
| C0265205 | Robinow Syndrome | DO | Noonan syndrome 8 | 0060586 |
| C0265205 | Robinow Syndrome | DO | Noonan syndrome 9 | 0060587 |
| C0265205 | Robinow Syndrome | DO | Noonan syndrome 10 | 0060588 |
| C0265205 | Robinow Syndrome | DO | microcephalic osteodysplastic primordial dwarfism type I | 0060608 |
| C0265205 | Robinow Syndrome | DO | microcephalic osteodysplastic primordial dwarfism type II | 0060609 |
| C0265205 | Robinow Syndrome | DO | autosomal dominant Robinow syndrome 2 | 0060765 |
| C0265205 | Robinow Syndrome | DO | autosomal dominant Robinow syndrome 1 | 0060766 |
| C0265205 | Robinow Syndrome | DO | autosomal dominant Robinow syndrome 3 | 0060767 |
| C0265205 | Robinow Syndrome | DO | Cornelia de Lange syndrome | 11725 |
| C0265205 | Robinow Syndrome | DO | Prader-Willi syndrome | 11983 |
| C0265205 | Robinow Syndrome | DO | Silver-Russell syndrome | 14681 |
| C0265205 | Robinow Syndrome | DO | Dubowitz syndrome | 14796 |
| C0265205 | Robinow Syndrome | DO | Cockayne syndrome | 2962 |
| C0265205 | Robinow Syndrome | DO | Noonan syndrome | 3490 |
| C0265205 | Robinow Syndrome | DO | Aarskog syndrome | 6683 |
| C0265205 | Robinow Syndrome | ICD10CM | Cockayne syndrome | Q87.1 |