All diseases

OMIM ID
605814
OMIM term:
CITRULLINEMIA, TYPE II, NEONATAL-ONSET
Alternative terms:

(∗) Location:
7q21.3  
(†) Associated OMIM genes:
SLC25A13  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/1h4ymr69