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Human Disease and Mouse Model Detail
Human Disease Diarrhea 2, with Microvillus Atrophy; DIAR2
OMIM ID: 251850
Human Phenotype Ontology associations
Synonyms Congenital Familial Protracted Diarrhea with Enterocyte Brush-Border Abnormalities; Davidson Disease; Diarrhea, Congenital; Intractable Diarrhea of Infancy; Microvillus Atrophy, Congenital; Microvillus Inclusion Disease; MVID
View all models View ALL (3) 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
     MYO5B* Myo5b* View 2 models HomoloGene and HGNC
     CDC42 Cdc42* View 1 model HGNC
References Disease References using Mouse Models (3)

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 6.06
The Jackson Laboratory