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Results 1 - 10 of 23 for Familial hypertrophic cardiomyopathy 9
  1. Familial hypertrophic cardiomyopathy 
    ... 18; CMH18 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9; CMH9 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21; CMH21 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  2. Familial dilated cardiomyopathy 
    ... JD. Update 2011: clinical and genetic issues in familial dilated cardiomyopathy. J Am Coll Cardiol. 2011 Apr 19;57(16):1641-9. doi: 10.1016/j.jacc.2011.01.015. ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  3. Arrhythmogenic right ventricular cardiomyopathy 
    ... 8 Genetic Testing Registry: Arrhythmogenic right ventricular dysplasia 9 ... ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3; ...
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
  4. ACAD9 deficiency 
    ... dehydrogenase 9 deficiency Deficiency of acyl-CoA dehydrogenase family member 9 Mitochondrial complex I deficiency due to ACAD9 deficiency ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  5. Keratoderma with woolly hair 
    ... HAIR AND KERATODERMA; DCWHK ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11 CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  6. Left ventricular noncompaction 
    ... Lorts A, Jefferies JL. Left ventricular non-compaction cardiomyopathy. Lancet. 2015 Aug 22;386(9995):813-25. doi: 10.1016/S0140-6736(14)61282-4. Epub 2015 Apr 9. Citation on PubMed Wang C, Takasaki A, Watanabe ...
    https://medlineplus.gov/.../condition/left-ventricular-noncompaction - Genetics
  7. Myhre syndrome 
    ... Wolf D, Callewaert B. Myhre syndrome: A first familial recurrence and broadening of the phenotypic spectrum. Am J Med Genet A. 2019 Dec;179(12):2494-2499. doi: 10.1002/ajmg.a.61377. Epub 2019 Oct 9. Citation on PubMed Michot C, Le Goff C, ...
    https://medlineplus.gov/genetics/condition/myhre-syndrome - Genetics
  8. Costello syndrome 
    ... this condition have short stature compared to their family and peers and may have ... Neurological problems in people with Costello syndrome include ...
    https://medlineplus.gov/genetics/condition/costello-syndrome - Genetics
  9. Catecholaminergic polymorphic ventricular tachycardia 
    ... by catecholamines Catecholamine-induced polymorphic ventricular tachycardia CPVT Familial polymorphic ventricular tachycardia FPVT ... PubMed ...
    https://medlineplus.gov/...ergic-polymorphic-ventricular-tachycardia - Genetics
  10. Rippling muscle disease 
    ... isolated hyperCKemia, and a heart disorder called hypertrophic cardiomyopathy. ... within the same family.Some people with rippling muscle disease do not ...
    https://medlineplus.gov/genetics/condition/rippling-muscle-disease - Genetics
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