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Last updated in GTR:
At a Glance
Intellectual disability, autosomal dominant 14; 3-methylcrotonyl-CoA carboxylase 2 deficiency; 3M syndrome 1; ...
ABAT (16p13.2), ABCA7 (19p13.3), ABCD1 (Xq28), ACE (17q23.3), ACHE (7q22.1), ...
Conditions Help
Total conditions: 777
Condition/Phenotype Identifier
Methodology
Total methods: 0
Method Category Help
Test method Help
Instrument *
* Instrument: Not provided
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Additional Information

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