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At a Glance
Limb-girdle muscular dystrophy-dystroglycanopathy, type C4; 2-methyl-3-hydroxybutyric aciduria; 22q13.3 deletion syndrome; ...
ABCC6 (16p13.11), ABCD1 (Xq28), ABCG5 (2p21), ACAT1 (11q22.3), ACOX1 (17q25.1), ...
Conditions Help
Total conditions: 750
Condition/Phenotype Identifier
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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