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CHDEPCC:10.10.20

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Hypertrophic cardiomyopathy

  Chromosomal map of CHD genes and imbalances.

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External references for Hypertrophic cardiomyopathy

  • Ncbi.png Search OMIM :
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Genes for phenotype 10.10.20:Hypertrophic cardiomyopathy

Non-syndromic

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Syndromic

  
 RAF1 edit association
  • Support: likely: 2 or more patients (with CHD and a mutation in the candidate gene)
  • References: PMID:22389993 (single case report modify)
  • Syndromes: LEOPARD syndrome 2 (LS-2) (OMIM:611554): a rare, dominantly inherited genetic disorder affecting multiple organ systems. The phenotypes include multiple lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormal genitalia, retardation of growth, and sensorineural deafness.
  • Incidence:
  • Comments:
  • Studies: (1)
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Regions for phenotype 10.10.20:Hypertrophic cardiomyopathy

Region Patients References OMIM Comments

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Translocations 10.10.20:Hypertrophic cardiomyopathy

Region References OMIM Comments

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Patients reports for 10.10.20:Hypertrophic cardiomyopathy


Automated text-mining genes found for 10.10.20:Hypertrophic cardiomyopathy

AGeneApart Method

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This page contributors

  • yaojuan jia - institute for human genetics (Belgium) (association)

  • Jeroen Breckpot - CME Leuven (Belgium) (study)


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