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Results 1 - 10 of 125 for Familial hypertrophic cardiomyopathy 1
  1. ... Organization for Rare Disorders (NORD) ClinicalTrials.gov CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1; RCM1 CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3; RCM3 CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 2; ...
  2. ... 4; CMH4 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; ...
  3. ... This Health Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition AD3 FAD presenilin 1 (Alzheimer disease 3) presenilin 1 protein PS1 PSN1_ ...
  4. ... DYSPLASIA, FAMILIAL, 3; ARVD3 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4; ARVD4 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5 ...
  5. ... HE, Kern M, Katus HA, Frey N. Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation. Cardiovasc Res. 2010 Jun 1;86(3):452-60. doi: 10.1093/cvr/ ...
  6. ... mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2). Hum Mol Genet. 2001 Feb 1;10(3):189-94. doi: 10.1093/hmg/ ...
  7. ... AV, Potter JD. Cellular and molecular aspects of familial hypertrophic cardiomyopathy caused by mutations in the cardiac troponin I gene. Mol Cell Biochem. 2004 Aug;263(1-2):99-114. doi: 10.1023/B:MCBI. ...
  8. ... 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 Gene ...
  9. ... This Health Condition MedlinePlus Genetics provides information about Familial restrictive cardiomyopathy More About This Health Condition beta-myosin heavy chain MGC138376 MGC138378 MPD1 MYH7_HUMAN MyHC-beta myhc-slow MYHCB myosin heavy chain (AA 1-96) Myosin heavy chain 7 Myosin heavy chain, ...
  10. ... This Health Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition AD3-like protein AD3L AD3LP AD4 AD5 Alzheimer's disease 3-like E5-1 presenilin 2 (Alzheimer disease 4) PS2 protein (alzheimer- ...
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