CUI Disease Vocabulary Name in Vocabulary Code
C0268542 Ornithine carbamoyltransferase deficiency DO ornithine carbamoyltransferase deficiency 9271
C0268542 Ornithine carbamoyltransferase deficiency EFO ornithine carbamoyltransferase deficiency 0007409
C0268542 Ornithine carbamoyltransferase deficiency ICD10CM Hyperammonemia-Hyperornithinemia-Homocitrullinemia syndrome E72.4
C0268542 Ornithine carbamoyltransferase deficiency ICD10CM Ornithine transcarbamylase deficiency E72.4
C0268542 Ornithine carbamoyltransferase deficiency MONDO ornithine carbamoyltransferase deficiency 0010703
C0268542 Ornithine carbamoyltransferase deficiency MSH Ornithine Carbamoyltransferase Deficiency Disease D020163
C0268542 Ornithine carbamoyltransferase deficiency MSH Ornithine Carbamoyltransferase Deficiency D020163
C0268542 Ornithine carbamoyltransferase deficiency NCI Ornithine Carbamoyltransferase Deficiency Disease C84957
C0268542 Ornithine carbamoyltransferase deficiency NCI Ornithine Transcarbamylase Deficiency C84957
C0268542 Ornithine carbamoyltransferase deficiency OMIM ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY 311250
C0268542 Ornithine carbamoyltransferase deficiency OMIM ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO 311250
C0268542 Ornithine carbamoyltransferase deficiency ORDO Ornithine transcarbamylase deficiency 664