Cardiomyopathy, familial hypertrophic, 23, with or without left ventricular non-compaction

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Subtype of: Cardiomyopathy · Hypertrophic cardiomyopathy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Cardiomyopathy, familial hypertrophic, 23, with or without left ventricular non-compaction
MONDO_0012808
ACTN2 Unknown
25173926 20022194 25224718
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Cardiomyopathy, familial hypertrophic, 23, with or without left ventricular non-compaction.
5 View disease cluster →
Cardiac and skeletal myopathy 1 shared geneACTN2 Related via 1 shared gene including ACTN2. Myopathy, congenital with structured cores and z-line abnormalities 1 shared geneACTN2 Related via 1 shared gene including ACTN2. Myopathy, distal, 6, adult onset 1 shared geneACTN2 Related via 1 shared gene including ACTN2. Cardiomyopathy, dilated, 1aa, with or without left ventricular non-compaction 1 shared geneACTN2 Related via 1 shared gene including ACTN2. Ventricular fibrillation 1 shared geneACTN2 Related via 1 shared gene including ACTN2.