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hypertrophic cardiomyopathy 14
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYH6 gene.
Uniprot Description A hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0110320
MESH:C567684
OMIM:613251
UMLS:C2750467
MONDO:0013197
High level summary of knowledge for a disease, including descriptions and datasource references.