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Summary Literature (0)
MIM:617047 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26; CMH26

Xenbase Genes: flnc

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014883 - distal epiphysis of distal phalanx of manual digit 3
MONDO:0019150 - obsolete familial isolated restrictive cardiomyopathy