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Summary Literature (0)
MIM:605814 - CITRULLINEMIA, TYPE II, NEONATAL-ONSET

Xenbase Genes: slc25a13

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011601 - neonatal intrahepatic cholestasis due to citrin deficiency

Disease Ontology (DO):
DOID:0070341 - neonatal-onset type II citrullinemia
DOID:9273 - citrullinemia