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At a Glance
Congenital myopathy with fiber type disproportion; Alpha-B crystallinopathy; Amyotrophic lateral sclerosis 20; ...
ACTA1 (1q42.13), AGL (1p21.2), AGRN (1p36.33), ALG14 (1p21.3), ALG2 (9q22.33), ...
Conditions Help
Total conditions: 148
Condition/Phenotype Identifier
Methodology
Total methods: 0
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Additional Information

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