| CUI | Disease | Vocabulary | Name in Vocabulary | Code |
|---|---|---|---|---|
| C1848199 | X-Linked Lissencephaly | MONDO | lissencephaly type 1 due to doublecortin gene mutation | 0010239 |
| C1848199 | X-Linked Lissencephaly | MSH | Syndrome, Miller-Dieker | D054221 |
| C1848199 | X-Linked Lissencephaly | MSH | Classical Lissencephaly | D054221 |
| C1848199 | X-Linked Lissencephaly | MSH | X-Linked Lissencephaly | D054221 |
| C1848199 | X-Linked Lissencephaly | MSH | Subcortical Band Heterotopia | D054221 |
| C1848199 | X-Linked Lissencephaly | MSH | Classical Lissencephalies and Subcortical Band Heterotopias | D054221 |
| C1848199 | X-Linked Lissencephaly | MSH | Lissencephaly, X-Linked, 1 | D054221 |
| C1848199 | X-Linked Lissencephaly | ORDO | Lissencephaly type 1 due to doublecortin gene mutation | 2148 |