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amelogenesis imperfecta hypomaturation type 2A4 (DOID:0110062)
Alliance: disease page
Synonyms: AI2A4; amelogenesis imperfecta hypomaturation type IIA4; amelogenesis imperfecta type IIA4
Alt IDs: OMIM:614832, ICD10CM:K00.5
Definition: An amelogenesis imperfecta caused by homozygous mutation in the C4ORF26 gene on chromosome 4q21.


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
12/13/2017
MGI 6.11
The Jackson Laboratory