Barth syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
BARTH SYNDROME
111302060MESH:D056889MONDO:0010543
TAFAZZIN Unknown
18430085 25185984 23843353 8630491
CTD, ClinGen, Disgenet, HPO, Orphanet
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Barth syndrome.
5 View disease cluster →
Left ventricular noncompaction cardiomyopathy 1 shared geneTAFAZZIN Related via 1 shared gene including TAFAZZIN. Left ventricular disease 1 shared geneTAFAZZIN Related via 1 shared gene including TAFAZZIN. Cardiomyopathy 1 shared geneTAFAZZIN Related via 1 shared gene including TAFAZZIN. Dilated cardiomyopathy 1 shared geneTAFAZZIN Related via 1 shared gene including TAFAZZIN. Coronary artery disease 1 shared geneTAFAZZIN Related via 1 shared gene including TAFAZZIN.