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Human Disease and Mouse Model Detail
Human Disease Combined Oxidative Phosphorylation Deficiency 3; COXPD3
OMIM ID: 610505
Synonyms Combined Oxidative Phosphorylation Deficiency; Concentric Cardiomyopathy, Hypotonia, and Lactic Acidosis; Encephalomyopathy, Respiratory Failure, and Lactic Acidosis
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
     TSFM* Tsfm   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 6.03
The Jackson Laboratory