All diseases

OMIM ID
215700
OMIM term:
CITRULLINEMIA, CLASSIC
Alternative terms:
CITRULLINEMIA, TYPE I; CTLN1
CITRULLINURIA
ARGININOSUCCINATE SYNTHETASE DEFICIENCY
ASS DEFICIENCY
(∗) Location:
9q34.11  
(†) Associated OMIM genes:
ASS1 ARGININOSUCCINATE SYNTHETASE PSEUDOGENES, INCLUDED  
(‡) Associated MGI genes:
Ass1  

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