The association between FHOD3 (Formin Homology 2 Domain Containing 3) and Cardiomyopathy, Familial Hypertrophic, 28 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and likely-pathogenic variants.
Sources3
Clinical variants38
Symptoms25
Compounds0
Trials0
Publications3
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.