Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Baylor Genetics | RCV000006364 | SCV004201696 | likely pathogenic | Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | 2022-05-07 | criteria provided, single submitter | clinical testing | |
OMIM | RCV000006364 | SCV000026546 | pathogenic | Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome | 2009-05-01 | no assertion criteria provided | literature only |