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At a Glance
Amyloidogenic transthyretin amyloidosis; Autosomal recessive limb-girdle muscular dystrophy type 2G; CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 27; ...
ACTC1 (15q14), ACTN2 (1q43), ALPK3 (15q25.3), ANKRD1 (10q23.31), BAG3 (10q26.11), ...
Conditions Help
Total conditions: 54
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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