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At a Glance
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5; Congenital disorder of glycosylation type 1E; Congenital disorder of glycosylation type 1O; ...
B3GALNT2 (1q42.3), B4GAT1 (11q13.2), DAG1 (3p21.31), DPM1 (20q13.13), DPM3 (1q22), ...
Conditions Help
Total conditions: 21
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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