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Human Disease and Mouse Model Detail
Human Disease

Term: AMME Complex
OMIM ID: 300194

Synonyms Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis; ATS-MR; Chromosome Xq22.3 Telomeric Deletion Syndrome
Associated Genes
 There are currently no human or mouse genes associated with this disease in the MGI database.
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
04/03/2013
MGI 5.12 		The Jackson Laboratory