About   Help   FAQ
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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Erbb2* ERBB2 View 1 model 1:1 Homology
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
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 5.21
The Jackson Laboratory