About   Help   FAQ
Disease Ontology Browser
amelogenesis imperfecta hypomaturation type 2A5 (DOID:0110063)
Synonyms: AI2A5; amelogenesis imperfecta hypomaturation type IIA5; amelogenesis imperfecta type IIA5
Alt IDs: OMIM:615887, ICD10CM:K00.5
Definition: An amelogenesis imperfecta that has material basis in homozygous mutation in the SLC24A4 gene on chromosome 14q32.


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
03/21/2017
MGI 6.08
The Jackson Laboratory