Congenital hyperammonemia, type I Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/237300
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Genes

1 genes associated with the Congenital hyperammonemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
CPS1 carbamoyl-phosphate synthase 1, mitochondrial