| CUI | Disease | Vocabulary | Name in Vocabulary | Code |
|---|---|---|---|---|
| C0268540 | HHH syndrome | DO | ornithine translocase deficiency | 0050720 |
| C0268540 | HHH syndrome | DO | ornithine carbamoyltransferase deficiency | 9271 |
| C0268540 | HHH syndrome | ICD10CM | Hyperammonemia-Hyperornithinemia-Homocitrullinemia syndrome | E72.4 |
| C0268540 | HHH syndrome | ICD10CM | Ornithine transcarbamylase deficiency | E72.4 |
| C0268540 | HHH syndrome | MONDO | ornithine translocase deficiency | 0009393 |
| C0268540 | HHH syndrome | MSH | HHH syndrome | C538380 |
| C0268540 | HHH syndrome | NCI | HHH | C129029 |
| C0268540 | HHH syndrome | NCI | Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome | C129029 |
| C0268540 | HHH syndrome | OMIM | HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME | 238970 |
| C0268540 | HHH syndrome | OMIM | HHH SYNDROME | 238970 |
| C0268540 | HHH syndrome | ORDO | Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | 415 |