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Summary Literature (0)
DOID:0110327 - hypertrophic cardiomyopathy 26

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the FLNC gene on chromosome 7q32.

Synonyms: cardiomyopathy familial hypertrophic 26, CMH26

Xenbase Genes : flnc

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014883 - distal epiphysis of distal phalanx of manual digit 3


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): familial hypertrophic cardiomyopathy (is_a), hypertrophic cardiomyopathy (is_a)