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Last updated in GTR:
At a Glance
Deficiency of acetyl-CoA acetyltransferase; Combined malonic and methylmalonic aciduria; Congenital disorder of glycosylation type 1t; ...
ACAT1 (11q22.3), ACSF3 (16q24.3), AGL (1p21.2), ALDOB (9q31.1), FBP1 (9q22.32), ...
Conditions Help
Total conditions: 23
Condition/Phenotype Identifier
Methodology
Total methods: 0
Method Category Help
Test method Help
Instrument *
* Instrument: Not provided
Technical Information
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Additional Information

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