All diseases

OMIM ID
237300
OMIM term:
CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO
Alternative terms:
CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY
CPS I DEFICIENCY
(∗) Location:
2q34  
(†) Associated OMIM genes:
CPS1 VENOOCCLUSIVE DISEASE AFTER BONE MARROW TRANSPLANTATION, SUSCEPTIBILITY TO, INCLUDED  
(‡) Associated MGI genes:
Cps1  

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* quick link - http://q.sanger.ac.uk/ik1l0wy4