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Human Disease and Mouse Model Detail
Human Disease Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1; CEMCOX1
OMIM ID: 604377
Human Phenotype Ontology associations
Synonyms Cardioencephalomyopathy, Fatal Infantile; Cytochrome C Oxidase Deficiency, Fatal Infantile, with Cardioencephalomyopathy
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
     SCO2* Sco2   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