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At a Glance
Familial hypertrophic cardiomyopathy 1; Amyloidogenic transthyretin amyloidosis; Atrial septal defect 3 more...
ACTC1 (15q14); ACTN2 (1q43); ALPK3 (15q25.3); ANKRD1 (10q23.31); CSRP3 (11p15.1) more...
Conditions Help
Total conditions: 59
Condition/Phenotype Identifier
Methodology
Total methods: 0
Method Category Help
Test method Help
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* Instrument: Not provided
Technical Information
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Additional Information

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