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Human Disease and Mouse Model Detail
Human Disease Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant; EDMD2
OMIM ID: 181350
Human Phenotype Ontology associations
Synonyms Emd2; Emery-Dreifuss Muscular Dystrophy; Emery-Dreifuss Muscular Dystrophy, Autosomal Dominant; Hauptmann-Thannhauser Muscular Dystrophy; Muscular Dystrophy with Early Contractures and Cardiomyopathy, Autosomal Dominant; Scapuloilioperoneal Atrophy with Cardiopathy
View all models View ALL (3) 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
     LMNA* Lmna* View 2 models HomoloGene and HGNC
     ZMPSTE24 Zmpste24* View 1 model HomoloGene and HGNC
References Disease References using Mouse Models (9)

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