Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:605814 - CITRULLINEMIA, TYPE II, NEONATAL-ONSET

Xenbase Genes: slc25a13

Human Disease Resource: OMIM

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