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Human Disease and Mouse Model Detail
Human Disease Diarrhea 2, with Microvillus Atrophy; DIAR2
OMIM ID: 251850
Synonyms Congenital Familial Protracted Diarrhea with Enterocyte Brush-Border Abnormalities; Davidson Disease; Intractable Diarrhea of Infancy; Microvillus Atrophy, Congenital; Microvillus Inclusion Disease; MVID
View all models View ALL (1) mouse models for this human disease.
Genes and
mouse models 		Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Cdc42* CDC42 View 1 model 1:1 Homology
     Myo5b MYO5B*   1:1 Homology
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
06/05/2013
MGI 5.13 		The Jackson Laboratory