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Human Disease and Mouse Model Detail
Human Disease Cardiomyopathy, Familial Hypertrophic, 1; CMH1
OMIM ID: 192600
Synonyms Asymmetric Septal Hypertrophy; ASH; Cardiomyopathy, Familial Hypertrophic; Cmh; Hypertrophic Subaortic Stenosis, Idiopathic; Ventricular Hypertrophy, Hereditary
View all models View ALL (2) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Pepd* PEPD View 1 model 1:1 Homology
     Cav3 CAV3*   1:1 Homology
Myh6 MYH6*   1:1 Homology
Myh7 MYH7*   1:1 Homology
Mylk2 MYLK2*   1:1 Homology
Transgenes and
other genome features
Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Tg(Myh6-Erbb2)6Kaga View 1 model
References Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/09/2014
MGI 5.20
The Jackson Laboratory