HCM | DCM | ARVC | Arrhythmogenic CM | RCM | Unclassified |
Familial, unknown gene Sarcomeric protein mutations
Glycogen storage disease (eg, Pompe; PRKAG2, Forbes, Danon) Lysosomal diseases (eg, Fabry, Hurler) Disorders of fatty acid metabolism Carnitine deficiency Phosphorylase B kinase deficiency Mitochondrial cytopathies Syndromic HCM
Other
| Familial, unknown gene Sarcomeric protein mutations (refer to HCM) Z-band
Cytoskeletal genes
Nuclear membrane
Mildly dilated CM Intercalated disc protein mutations (refer to ARVC) Mitochondrial cytopathy | Familial, unknown gene Intercalated disc protein mutations
Transmembrane protein 43 (TMEM43) | Familial, unknown gene Intercalated disc protein mutations (refer to ARVC) Lamin A/C SCN5A Phospholamban FLNC Desmin | Familial, unknown gene Sarcomeric protein mutations
Familial amyloidosis
Desminopathy Pseuxanthoma elasticum Haemochromatosis Fabry disease Glycogen storage disease | Left ventricular noncompaction
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