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Human Disease and Mouse Model Detail
Human Disease Cardiomyopathy, Familial Hypertrophic, 1; CMH1
OMIM ID: 192600
Human Phenotype Ontology associations
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...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     PEPD Pepd* View 1 model HomoloGene and HGNC
     CAV3* Cav3   HomoloGene and HGNC
MYH6* Myh6   HomoloGene and HGNC
MYH7* Myh7   HomoloGene and HGNC
MYLK2* Mylk2   HomoloGene and HGNC
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
MGI 6.07
The Jackson Laboratory