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Human Disease and Mouse Model Detail
Human Disease Emery-Dreifuss Muscular Dystrophy 1, X-Linked; EDMD1
OMIM ID: 310300
Human Phenotype Ontology associations
Synonyms EMD1; Emery-Dreifuss Muscular Dystrophy; Humeroperoneal Neuromuscular Disease, Formerly; Muscular Dystrophy, Tardive, Dreifuss-Emery Type, with Contractures; Scapuloperoneal Syndrome, X-Linked, Formerly
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
     EMD* Emd   HomoloGene and HGNC

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