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Results 1 - 10 of 53 for Familial syndrome associated with hypertrophic cardiomyopathy
  1. Causes of Cardiomyopathy (Children's Cardiomyopathy Foundation)  
    Cardiomyopathy/Children ... Cardiomyopathy ... Children's Cardiomyopathy Foundation
    https://www.childrenscardiomyopathy.org/pages/about-disease/causes - External Health Links
  2. Familial dilated cardiomyopathy 
    ... an identified mutation in any of the known associated genes. The cause of the ... occur as part of syndromes that affect other organs and tissues in the ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  3. Alström syndrome 
    ... Jacobson Z, Young TL, Marshall JD, Kaplan P. Familial variable expression of dilated cardiomyopathy in Alstrom syndrome: a report of four sibs. Am J Med ...
    https://medlineplus.gov/genetics/condition/alstrom-syndrome - Genetics
  4. Myoclonic epilepsy with ragged-red fibers 
    ... mitochondrial gene and occurs in people with no family history of MERRF. Fukuhara disease MERRF MERRF syndrome Myoclonic epilepsy associated with ragged-red fibers Myoencephalopathy ragged-red fiber ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  5. SCN5A gene 
    ... SODIUM VOLTAGE-GATED CHANNEL, ALPHA SUBUNIT 5; SCN5A CARDIOMYOPATHY, DILATED, 1E; CMD1E SUDDEN INFANT DEATH SYNDROME VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 1; VF1 ATRIAL FIBRILLATION, FAMILIAL, 10; ATFB10 NCBI ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  6. Noonan syndrome 
    ... the lungs (pulmonary valve stenosis). Some have hypertrophic cardiomyopathy, which enlarges and weakens the heart muscle.A variety of bleeding disorders have been associated with Noonan syndrome. Some affected individuals have excessive bruising, nosebleeds, or ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  7. PRKAG2 gene 
    ... rhythms (arrhythmias) in people with Wolff-Parkinson-White syndrome. More About This Health Condition ... More About This Health Condition Several mutations in ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  8. Keratoderma with woolly hair 
    ... keratoderma syndrome Genetic Testing Registry: Naxos disease ... RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11 CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  9. FKTN gene 
    ... This Health Condition MedlinePlus Genetics provides ... gene can also cause Walker-Warburg syndrome, a severe form of congenital muscular dystrophy that ...
    https://medlineplus.gov/genetics/gene/fktn - Genetics
  10. MYH6 gene 
    ... This Health Condition MedlinePlus Genetics provides ... atria). Most of the MYH6 gene mutations associated with ASD affect a part of the α- ...
    https://medlineplus.gov/genetics/gene/myh6 - Genetics
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