argininosuccinic aciduria Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An amino acid metabolic disorder that involves the accumulation of argininosuccinic acid (ASA) in the blood and urine. (Human Disease Ontology, DOID_14755)
External Link http://www.omim.org/entry/207900
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Genes

1 genes associated with the argininosuccinic aciduria phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ASL argininosuccinate lyase