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Q33804620-2DD2F524-9102-4702-9D0D-BC110CEA456B
Q33804620-2DD2F524-9102-4702-9D0D-BC110CEA456B
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Statement
http://www.wikidata.org/entity/statement/Q33804620-2DD2F524-9102-4702-9D0D-BC110CEA456B
Significant hepatic involvement in patients with ornithine transcarbamylase deficiency.
P2860
Q33804620-2DD2F524-9102-4702-9D0D-BC110CEA456B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33804620-2DD2F524-9102-4702-9D0D-BC110CEA456B
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wasDerivedFrom
424fc289bf78754cb97f571a28ea28d814461f09
P2860
Liver failure with coagulopathy, hyperammonemia and cyclic vomiting in a toddler revealed to have combined heterozygosity for genes involved with ornithine transcarbamylase deficiency and Wilson disease.