Hyperornithinemia-hyperammonemia-homocitrullinuria Syndrome
| Disease Aliases (10) | Hhh - hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Hhh syndrome Hhhs Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome Hyperornithinemia-hyperammonemia-homocitrullinuria (hhh) syndrome Ornithine carrier deficiency Ornithine translocase deficiency Ornt1 deficiency Slc25a15-gene related hyperornithinemia, hyperammonemia, homocitrullinuria syndrome Solute carrier family 25 member 15-gene related hyperornithinemia, hyperammonemia, homocitrullinuria syndrome |
Associated Genes (0) | |||||||
| Cross-references of Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |