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Human Disease and Mouse Model Detail
Human Disease Myopathy Due to Myoadenylate Deaminase Deficiency; MMDD
OMIM ID: 615511
Human Phenotype Ontology associations
Synonyms Adenosine Monophosphate Deaminase-1 Deficiency, Myopathy Due to; Ampd1 Deficiency; Myoadenylate Deaminase Deficiency, Myopathy Due to
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
     AMPD1* Ampd1   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