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Human Disease and Mouse Model Detail
Human Disease Myopathy, Myofibrillar, 1; MFM1
OMIM ID: 601419
Human Phenotype Ontology associations
Synonyms Arrhythmogenic Right Ventricular Cardiomyopathy 7, Formerly; ARVC7, FORMERLY; Arrhythmogenic Right Ventricular Dysplasia, Familial, 7, Formerly; ARVD7, FORMERLY; Cardiomyopathy, Dilated, 1f and Limb-Girdle Muscular Dystrophy Type 1d, Formerly; Cardiomyopathy, Dilated, with Conduction Defect and Muscular Dystrophy; CDCD3, FORMERLY; Cmd1f and Lgmd1d, Formerly; Desmin-Related Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy; Desmin-Related Myopathy; DRM; Desminopathy, Primary; Inclusion Body Myopathy 1, Autosomal Dominant, Formerly; IBM1, FORMERLY; Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy; Myopathy, Myofibrillar; Myopathy, Myofibrillar, Desmin-Related
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
     DES* Des* View 1 model HomoloGene and HGNC
     LDB3 Ldb3* View 1 model HomoloGene and HGNC
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