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At a Glance
Malouf syndrome; Amyloidogenic transthyretin amyloidosis; Benign scapuloperoneal muscular dystrophy with cardiomyopathy more...
AARS (16q22.1); ATL1 (14q22.1); DNM2 (19p13.2); DNMT1 (19p13.2); DYNC1H1 (14q32.31) more...
Conditions Help
Total conditions: 90
Condition/Phenotype Identifier
Methodology
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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