Hyperornithinemia-hyperammonemia-homocitrullinuria Syndrome
| Disease Aliases (13) | Hhh Hhh - hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Hhh syndrome Hhhs Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome Hyperornithinemia-hyperammonemia-homocitrullinuria (hhh) syndrome Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Ornithine translocase deficiency Ornt1 deficiency Ornithine carrier deficiency Ornithine translocase deficiency syndrome Triple h syndrome |
Associated Genes (1) NCBI-RefSeq: SLC25A15 (Solute carrier family 25 member 15) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |