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Human Disease and Mouse Model Detail
Human Disease Corneal Dystrophy, Posterior Polymorphous, 1; PPCD1
OMIM ID: 122000
Human Phenotype Ontology associations
Synonyms Corneal Dystrophy, Hereditary Polymorphous Posterior; Corneal Endothelial Dystrophy 1, Autosomal Dominant, Formerly; CHED1, FORMERLY; Maumenee Corneal Dystrophy; Posterior Polymorphous Corneal Dystrophy; PPCD
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
     OVOL2* Ovol2   HomoloGene and HGNC
VSX1* Vsx1   HomoloGene and HGNC
Transgenes and
other genome features
Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Dp(2Csrp2bp-Dzank1)1Bra View 2 models
References Disease References using Mouse Models (1)

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