About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Amelogenesis Imperfecta, Type III; AI3
OMIM ID: 130900
Synonyms Amelogenesis Imperfecta; Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Dominant; ADHCAI; Amelogenesis Imperfecta, Hypomineralization Type
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...
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Fam83h FAM83H*   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
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
04/21/2015
MGI 5.21
The Jackson Laboratory