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Summary Literature (0)
MIM:311250 - ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO

Xenbase Genes: otc

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010703 - ornithine carbamoyltransferase deficiency

Disease Ontology (DO):
DOID:9271 - ornithine carbamoyltransferase deficiency