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Human Disease and Mouse Model Detail
Human Disease Kearns-Sayre Syndrome; KSS
OMIM ID: 530000
Human Phenotype Ontology associations
Synonyms Chronic Progressive External Ophthalmoplegia with Myopathy; CPEO with Myopathy; CPEO with Ragged-Red Fibers; Mitochondrial Cytopathy; Oculocraniosomatic Syndrome; Ophthalmoplegia, Pigmentary Degeneration of Retina, and Cardiomyopathy; Ophthalmoplegia, Progressive External, with Ragged-Red Fibers; Ophthalmoplegia-Plus Syndrome
View all models View ALL (2) 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
     TFAM Tfam* View 2 models HomoloGene and HGNC
References Disease References using Mouse Models (2)

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